Bispecific and monospecific antibodies using novel anti-pd-1 sequences

ABSTRACT

The present invention is directed to bispecific, heterodimeric checkpoint antibodies.

I. PRIORITY CLAIM

This application is a continuation of U.S. patent application Ser. No. 16/184,895, filed Nov. 8, 2018 which claims priority to United States Patent Application Nos. 62/583,438, filed Nov. 8, 2017; 62/598,938, filed Dec. 14, 2017 and 62/658,227, filed Apr. 16, 2018 all of which are expressly incorporated herein by reference in their entirety, with particular reference to the figures, legends, and claims therein.

II. SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on May 7, 2019, is named 067461-5215-WO_SL_v2.txt and is 39,084,712 kilobytes in size.

III. BACKGROUND OF THE INVENTION

Checkpoint receptors such as CTLA-4, PD-1 (programmed cell death 1), TIM-3 (T cell immunoglobulin and mucin domain 3), LAG-3 (lymphocyte-activation gene 3), TIGIT (T cell immunoreceptor with Ig and ITIM domains), and others, inhibit the activation, proliferation, and/or effector activities of T cells and other cell types. Guided by the hypothesis that checkpoint receptors suppress the endogenous T cell response against tumor cells, preclinical and clinical studies of anti-CTLA4 and anti-PD1 antibodies, including nivolumab, pembrolizumab, ipilimumab, and tremelimumab, have indeed demonstrated that checkpoint blockade results in impressive anti-tumor responses, stimulating endogenous T cells to attack tumor cells, leading to long-term cancer remissions in a fraction of patients with a variety of malignancies. Unfortunately, only a subset of patients responds to these therapies, with response rates generally ranging from 10 to 30% and sometimes higher for each monotherapy, depending on the indication and other factors. Therapeutic combination of these agents, for example ipilimumab plus nivolumab, leads to even higher response rates, approaching 60% in some cases. Preclinical studies have shown additional synergies between anti-PD-1 antibodies and/or anti-CTLA-4 antibodies with blockade of more recently identified checkpoint receptors, including LAG-3, TIM-3, BTLA and TIGIT. While the potential of multiple checkpoint blockade is very promising, combination therapy with such agents is expected to carry a high financial burden. Moreover, autoimmune toxicities of combination therapies, for example nivolumab plus ipilimumab, are significantly elevated compared to monotherapy, causing many patients to halt the therapy.

A number of studies (Ahmadzadeh et al., Blood 114:1537 (2009), Matsuzaki et al., PNAS 107(17):7875-7880 (2010), Fourcade et al., Cancer Res. 72(4):887-896 (2012) and Gros et al., J. Clinical Invest. 124(5):2246 (2014)) examining tumor-infiltrating lymphocytes (TILs) have shown that TILs commonly express multiple checkpoint receptors. Moreover, it is likely that TILs that express multiple checkpoints are in fact the most tumor-reactive. In contrast, non-tumor reactive T cells in the periphery are more likely to express a single checkpoint. Checkpoint blockade with monospecific full-length antibodies is likely nondiscriminatory with regards to de-repression of tumor-reactive TILs versus autoantigen-reactive single expressing T cells that are assumed to contribute to autoimmune toxicities.

Accordingly, the invention is directed to bispecific antibodies that bind to human PD-1 and a second, different checkpoint inhibitor protein. Also provided are monospecific monoclonal antibodies that bind to human PD-1.

IV. BRIEF SUMMARY OF THE INVENTION

The present invention is directed to novel anti-PD-1 antigen binding domains (ABDs) and their uses in the creation of anti-PD-1 monovalent monoclonal antibodies and heterodimeric, bispecific antibodies that bind to PD-1 and a second target antigen selected from the group consisting of CTLA-4, LAG-3, TIM-3, TIGIT, BTLA and ICOS, and methods of making and using the antibodies.

Accordingly, in some aspects the invention provides anti-PD-1 monovalent monoclonal antibodies. In this aspect, the anti-PD-1 monoclonal antibody comprising: a) a heavy chain comprising, from N- to C-terminal, VH-CH1-hinge-CH2-CH3; and b) a light chain comprising, from N- to C-terminal, VL-CL; wherein the VHCDR1, VHCDR2, VHCDR3, VLCDR1, VLCDR2 and VLCDR3 are selected from the group consisting of the CDRs from XENP26940 in FIG. 24 and the CDRs from XNE28652 in FIG. 40.

In an additional aspect, the antibody has a VH and VL from XENP26940 depicted in FIG. 24.

In a further aspect, the antibody has a VH and VL from XENP28652 depicted in FIG. 40.

In either aspect, the hinge-CH2-CH3 can be an Fc domain selected from the group consisting of the Fc domain from human IgG1, IgG2, IgG3 and IgG4. When from IgG1, the Fc domain can be a variant human IgG1 domain, for example including the amino acid substitutions 427L/434S. Additionally, the variant IgG1 Fc domain can comprise ablation variants selected from those depicted in FIG. 5, and in particular the E233P/L234V/L235A/G236del/S267K substitutions. When the Fc domain is a variant human IgG4 domain it can comprise an S228P amino acid substitution.

In further aspects, the invention provides nucleic acid compositions comprising a first nucleic acid encoding the heavy chain and a second nucleic acid encoding the light chain. Also included are expression vector compositions comprising a first expression vector comprising the first nucleic acid and a second expression vector comprising said second nucleic acid, or a single expression vector comprising said first and second nucleic acids. Further included are host cells comprising the expression vector composition or expression vectors. Methods of making the anti-PD-1 antibodies are also included, comprising culturing the host cells under conditions wherein said antibody is expressed, and recovering said antibody. Furthermore, the invention provides methods of treating cancer in a patient in need thereof comprising administering the antibody to said patient.

In a further aspect, heterodimeric bispecific antibodies are provided. These antibodies comprise: a) a first monomer comprising: i) a single chain Fv domain (scFv) that binds human PD-1, wherein said scFv domain comprises: 1) a first variable heavy domain (VH1); 2) a scFv linker; and 3) a first variable light domain (VL1); and ii) a first variant Fc domain; b) a second monomer comprising: i) a heavy chain comprising a second variable heavy domain (VH2)-CH1-hinge-CH2-CH3; and c) a light chain comprising a second variable light domain (VL2) and a constant light domain (CL); wherein said first variable heavy domain and said first variable light domain form a first antigen binding domain (ABD1) and wherein said second variable heavy domain and said second variable light domain form a second ABD (ABD2) that binds to an antigen selected from human CTLA-4, human LAG-3, human TIM-3, human TIGIT, human BTLA and human ICOS. ABD1 can be any of the 1C11 VH and VL domains as outlined in FIGS. 13, 15, 16, 18, 20, 21, 24, 33 and 40.

In particular aspects, the ABD1 has sequences selected from the pairs consisting of 1C11[PD-1]_H3.234_L3.144 from XENP25806 in FIG. 15, 1C11[PD-1]_H3.240_L3.148 from XENP25812 from FIG. 15, 1C11[PD-1]_H3.241_L3.148 from XENP25813 in FIG. 15 and 1C11[PD-1]_H3.241_L3.92 from XENP25819 in FIG. 15.

In these aspects, the first monomer can comprise, from N- to C-terminal, VH1-scFv linker-VL1-hinge-variant Fc domain.

In further aspects, the first monomer can comprise, from N- to C-terminal, VL1-scFv linker-VH1-hinge-variant Fc domain.

In particular aspects, the ABD1 has sequences selected from the pairs consisting of 1C11[PD-1]_H3.234_L3.144 from XENP25806 in FIG. 15, 1C11[PD-1]_H3.240_L3.148 from XENP25812 from FIG. 15, 1C11[PD-1]_H3.241_L3.148 from XENP25813 in FIG. 15 and 1C11[PD-1]_H3.241_L3.92 from XENP25819 in FIG. 15, and the ABD2 binds to an antigen selected from human CTLA-4, human LAG-3, human TIM-3, human TIGIT, human BTLA and human ICOS.

In an additional aspect, the anti-CTLA-4 ABD2 has sequences selected from the pairs of SEQ ID NOs:38134 and 38138, 36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807, and 36811 and 36815 of the sequence listing.

In an additional aspect, the anti-LAG-3 ABD2 has sequences selected from the pairs of SEQ ID NOs:32755 and 32760, 36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959.

In an additional aspect, the anti-TIM-3 ABD2 has sequences selected from the pairs of SEQ ID NOs:36508 and 36513, 35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695.

In an additional aspect, the anti-TIGIT ABD2 has sequences selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583.

In an additional aspect, the anti-ICOS ABD2 has sequences selected from the group consisting of: a) the pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501; b) the VH and VL sequences of XENCS500 in FIG. 49; and c) the VH and VL sequences of XENCS501 in FIG. 49.

In an additional aspect, the anti-BTLA ABD2 has sequences selected from the pairs of SEQ ID NOs:20936 and 20941, 36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735.

In many aspects, the heterodimeric antibodies of the invention have a second variant IgG1 Fc domain comprises amino acid substitutions N208D/Q295E/N384D/Q418E/N421D, wherein said first and second variant IgG1 Fc domains each comprise amino acid substitutions E233P/L234V/L235A/G236del/S267K; and wherein said first variant IgG1 Fc domain comprises amino acid substitutions S364K/E357Q and second variant IgG1 Fc domain comprises amino acid substitutions L368D/K370S, wherein numbering is according to the EU index as in Kabat.

In further aspects, the invention provides nucleic acid compositions comprising: a) a first nucleic acid encoding said first monomer; b) a second nucleic acid encoding said second monomer; and c) a third nucleic acid encoding said light chain of any of claims 15 to 30.

In an additional aspect, the invention provides expression vector compositions comprising: a) a first expression vector comprising said first nucleic acid; b) a second expression vector comprising said second nucleic acid; and c) a third expression vector comprising said third nucleic acid. Also provided are host cells comprising the expression vector compositions, and methods of making the antibodies by culturing the host cells under conditions wherein said antibody is expressed, and recovering said antibody. Further provided are methods of treating cancer in a patient in need thereof comprising administering the heterodimeric bispecific antibodies of the invention to a patient.

V. BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A to 1O depict several formats of the present invention. The first is the “bottle opener” format, with a first and a second anti-antigen binding domain. Additionally, mAb-Fv, mAb-scFv, Central-scFv, Central-Fv, one armed central-scFv, one scFv-mAb, scFv-mAb, a dual scFv format, DVD-Ig, Trident and mAb-(scFv2) are all shown. For all of the scFv domains depicted, they can be either N- to C-terminus variable heavy-(optional linker)-variable light, or the opposite. In addition, for the one armed scFv-mAb, the scFv can be attached either to the N-terminus of a heavy chain monomer or to the N-terminus of the light chain.

FIGS. 2A to 2D depicts the antigen sequences for a number of antigens of use in the invention, including both human and cynomolgus monkey in many cases, to facilitate the development of antigen binding domains that bind to both for ease of clinical development. Unless otherwise stated, all references to these antigens are to the human antigen. The sequence of human ICOS (sp|Q9Y6W8) is shown in SEQ ID NO: 26246 of WO/2018/045110. The sequence of human ICOS, extracellular domain (sp|Q9Y6W8|21-140) is SEQ ID NO: 26247 of WO/2018/045110.

FIG. 3A to 3F depict useful pairs of heterodimerization variant sets (including skew and pI variants). On FIG. 3E, there are variants for which there are no corresponding “monomer 2” variants; these are pI variants which can be used alone on either monomer, or included on the Fab side of a bottle opener, for example, and an appropriate charged scFv linker can be used on the second monomer that utilizes a scFv as the second antigen binding domain. Suitable charged linkers are shown in FIG. 7.

FIG. 4 depict a list of isosteric variant antibody constant regions and their respective substitutions. pI_(−) indicates lower pI variants, while pI_(+) indicates higher pI variants. These can be optionally and independently combined with other heterodimerization variants of the invention (and other variant types as well, as outlined herein).

FIG. 5 depict useful ablation variants that ablate FcγR binding (sometimes referred to as “knock outs” or “KO” variants). Generally, ablation variants are found on both monomers, although in some cases they may be on only one monomer.

FIGS. 6A and 6B show two particularly useful embodiments of the invention.

FIGS. 7A and 7B depict a number of charged scFv linkers that find use in increasing or decreasing the pI of heterodimeric antibodies that utilize one or more scFv as a component. The (+H) positive linker finds particular use herein, particularly with anti-CD3 vl and vh sequences shown herein. A single prior art scFv linker with a single charge is referenced as “Whitlow”, from Whitlow et al., Protein Engineering 6(8):989-995 (1993). It should be noted that this linker was used for reducing aggregation and enhancing proteolytic stability in scFvs.

FIG. 8 depicts a list of engineered heterodimer-skewing Fc variants with heterodimer yields (determined by HPLC-CIEX) and thermal stabilities (determined by DSC). Not determined thermal stability is denoted by “n.d.”.

FIG. 9 depicts the sequences for XENP21575, a chimeric anti-PD-1 antibody based on the variable regions of hybridoma clone 1C11 and human IgG1 with E233P/L234V/L235A/G236del/S267K substitutions in the heavy chain. The CDRs are in bold, and the slashes indicate the borders of the variable domains. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VH and VL domain has its own SEQ ID NO: in the sequence listing.

FIG. 10 depicts blocking of PD-1/PD-L1 interaction on PD-1 transfected HEK293T cells by anti-PD-1 clone 1C11.

FIG. 11 depicts the binding of anti-PD-1 clone 1C11 to SEB-stimulated T cells.

FIGS. 12A and 12B depict cytokine release assays (A: IL-2; B: IFNγ) after SEB stimulation of human PBMCs and treatment with anti-PD-1 clone 1C11.

FIGS. 13A to 13C depict the sequences for illustrative Fab humanized variants of anti-PD-1 clone 1C11 in the human IgG1 format with E233P/L234V/L235A/G236del/S267K substitutions in the heavy chain. The CDRs are in bold, and the slashes indicate the borders of the variable domains. As note herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems. As will be appreciated by those in the art, the VH and VL domains can be formatted as Fab or scFvs. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VH and VL domain has its own SEQ ID NO: in the sequence listing.

FIG. 14 depicts the affinity of XENP22553 for PD-1 as determined by Octet (as well as the associated sensorgram).

FIG. 15A to 15T depict sequences for illustrative scFv variants of anti-PD-1 clone 1C11. The CDRs are underlined, the scFv linker is double underlined (in the sequences, the scFv linker is a positively charged scFv (GKPGS)4 linker, although as will be appreciated by those in the art, this linker can be replaced by other linkers, including uncharged or negatively charged linkers), and the slashes indicate the borders of the variable domains. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on numbering used as is shown in Table 1 and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems. Further, the naming convention illustrates the orientation of the scFv from N- to C-terminus; some of the sequences in this Figure are oriented as VH-scFv linker-VL (from N- to C-terminus), while some are oriented as VL-scFv linker-VH (from N- to C-terminus), although as will be appreciated by those in the art, these sequences may also be used in the opposition orientation from their depiction herein. Furthermore, as will be appreciated by those in the art, the VH and VL domains can be formatted as Fabs or scFvs. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VH and VL domain has its own SEQ ID NO: in the sequence listing.

FIGS. 16A and 16H depict sequences for illustrative variant anti-PD-1 mAbs with VH and VL domains from selected scFvs as described in Example XD. The CDRs are in bold, and the slashes indicate the borders of the variable domains. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems. As will be appreciated by those in the art, the VH and VL domains can be formatted as Fabs or scFvs. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VH and VL domain has its own SEQ ID NO: in the sequence listing.

FIG. 17A to 17Q depict the stability of variant anti-PD-1 scFvs as determined by DSF and equilibrium dissociation constants (KD), association rates (ka), and dissociation rates (kd) of anti-PD-1 mAbs based on the VH/VL from the variant scFvs as determined by Octet. XENP for scFvs are in bold, and XENP for full-length mAb are in parentheses.

FIGS. 18A to 18G depict sequences for illustrative variant anti-PD-1 mAbs based on clone 1C11. The CDRs are in bold, and the slashes indicate the borders of the variable domains. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems. As will be appreciated by those in the art, the VH and VL domains can be formatted as Fabs or scFvs. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VH and VL domain has its own SEQ ID NO: in the sequence listing.

FIG. 19 depicts the of equilibrium dissociation constants (KD), association rates (ka), and dissociation rates (kd) of variant anti-PD-1 mAbs as determined by Octet.

FIGS. 20A to 20L depict sequences for variant heavy chains based on the heavy chain of XENP22553. The CDRs are in bold. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH domain. As will be appreciated by those in the art, the VH domains can be used in Fabs or scFvs. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VH domain has its own SEQ ID NO: in the sequence listing.

FIGS. 21A to 21G depict sequences for variant light chains based on the light chain of XENP22553. The CDRs are in bold. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VL domains using other numbering systems. As will be appreciated by those in the art, the VL domains can be used in Fabs or scFvs. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VL domain has its own SEQ ID NO: in the sequence listing.

FIGS. 22A to 22E depict the of equilibrium dissociation constants (KD), association rates (ka), and dissociation rates (kd) of variant anti-PD-1 mAbs as determined by Octet. Variants are defined by heavy chain and light chain XenDs as depicted in FIGS. 20A-20L and FIGS. 21A-21G.

FIG. 23 depicts the of equilibrium dissociation constants (KD), association rates (ka), and dissociation rates (kd) of variant anti-PD-1 mAbs as determined by Octet. Variants are defined by heavy chain and light chain XenDs as depicted in FIG. 20 and FIG. 21.

FIGS. 24A to 24J depict sequences for additional illustrative variant anti-PD-1 mAbs based on clone 1C11. The CDRs are underlined, and the slashes indicate the borders of the variable domains. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems. As will be appreciated by those in the art, the VH and VL domains can be formatted as Fabs or scFvs. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VH and VL domain has its own SEQ ID NO: in the sequence listing.

FIG. 25 depicts the of equilibrium dissociation constants (KD), association rates (ka), and dissociation rates (kd) of variant anti-PD-1 mAbs as determined by Octet.

FIG. 26 depicts the affinity (KD) of anti-PD-1 1C11 variants as determined by Biacore.

FIG. 27 depicts the binding of affinity optimized anti-PD-1 1C11 variants to SEB-stimulated T cells.

FIG. 28 depicts the blocking of PD-L1 and PD-L2 binding to PD-1 by anti-PD-1 1C11 variants as determined by normalized BLI-response in a tandem epitope binning assay using Octet.

FIG. 29 depicts IFNγ secretion in an SEB-stimulated PBMC assay following incubation with the indicated test articles.

FIG. 30 depicts IFNγ secretion in an SEB-stimulated PBMC assay following incubation with the indicated test articles.

FIG. 31 depicts IFNγ secretion in an MLR assay following incubation with 20 μg/mL of the indicated test articles.

FIG. 32 depicts IFNγ secretion in an MLR assay following incubation with the indicated concentrations of the indicated test articles.

FIG. 33 depicts the sequences for XENP26842, a bivalent anti-PD-1 mAb with an ablation variant (E233P/L234V/L235A/G236del/S267K, “IgG1_PVA_/S267k”) and Xtend variant (M428L/N434S). The CDRs are underlined. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on the numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VH and VL domain has its own SEQ ID NO: in the sequence listing.

FIG. 34 depicts CD45⁺ cell counts in whole blood of NSG mice on Day 14 after engraftment with human PBMCs on Day 0 and dosing with indicated test articles on Days 1 and 8.

FIG. 35 depicts IFNγ concentration in serum of NSG mice on Day 7 after engraftment with human PBMCs on Day 0 and dosing with indicated test articles on Day 1.

FIGS. 36A and 36B depict A) the mean tumor volume and B) change in tumor volume in NSG mice engrafted with pp65-expressing MCF-7 cells, following engraftment with pp65 reactive huPBMC and treatment with indicated test articles.

FIGS. 37A to 37D depict A) CD45⁺ cell, B) CD4⁺ T cell, C) CD8⁺ T cell, and D) NK cell counts in the whole blood of NSG mice engrafted with pp65-expressing MCF-7 cells following engraftment with pp65 reactive huPBMC and treatment with indicated test articles.

FIG. 38 depicts the change in weight over time (as a percentage of initial body weight) in huPBMC-engrafted NSG mice dosed with the indicated test articles.

FIGS. 39A to 39C depict A) human CD45⁺, B) human CD4⁺ T cell, and C) human CD8⁺ T cell counts in huPBMC-engrafted NSG mice following dosing with the indicating test articles.

FIGS. 40A to 40BB depict sequences for additional illustrative variant anti-PD-1 mAbs based on clone 1C11. The CDRs are underlined, and the slashes indicate the borders of the variable domains. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems. As will be appreciated by those in the art, the VH and VL domains can be formatted as Fabs or scFvs. Additionally, these sequences can include the M428L/N434S Xtend mutations. Additionally, each CDR has its own SEQ ID NO: in the sequence listing, and each VH and VL domain has its own SEQ ID NO: in the sequence listing.

FIG. 41 depicts the affinity/dissociation constants (K_(D)), association rates (k_(a)), and dissociation rates (k_(d)) of anti-PD-1 1C11 variants for human PD-1 as determined by Octet.

FIG. 42 depicts the affinity/dissociation constants (K_(D)), association rates (k_(a)), and dissociation rates (k_(d)) of anti-PD-1 1C11 variants for human PD-1 as determined by Octet.

FIG. 43 depicts the affinity/dissociation constants (K_(D)), association rates (k_(a)), and dissociation rates (k_(d)) of anti-PD-1 1C11 variants for human PD-1 as determined by Octet.

FIG. 44 depicts the affinity/dissociation constants (K_(D)), association rates (k_(a)), and dissociation rates (k_(d)) of anti-PD-1 1C11 variants for human PD-1 as determined by Octet.

FIG. 45 depicts the affinity/dissociation constants (K_(D)), association rates (k_(a)), and dissociation rates (k_(d)) of anti-PD-1 1C11 variants for human PD-1 and cynomolgus PD-1 as determined by Octet.

FIG. 46 depicts the induction of IFNγ by indicated 1C11 variants (as well as PBS and anti-PD-1 XENP16432 based on nivolumab as controls) in an SEB-stimulated PBMC assay. p-values are from paired t-test, comparing IFNγ secretion by PBMCs from the same donor.

FIG. 47 depicts the induction of IL-2 by indicated 1C11 variants (as well as PBS and anti-PD-1 XENP16432 based on nivolumab as controls) in an SEB-stimulated PBMC assay. p-values are from paired t-test, comparing IL-2 secretion by PBMCs from the same donor.

FIG. 48 depicts the induction of IFNγ by indicated anti-PD-1 mAb XENP16432 based on nivolumab and XENP28652 in an SEB-stimulated PBMC assay. p-values are from paired t-test, comparing IFNγ secretion by PBMCs from the same donor.

FIGS. 49A to 49KK show the sequences of a number of heterodimeric antibodies of the present invention in the “bottle opener” format, named using “XENCS” numbering. Three polypeptide chains are shown for each (“Fab chain, scFv chain and light chain”), with the CDRs underlined, linkers double underlined, and the junction between domains indicated by a “/”. Each of these has its own sequence and thus identifier.

FIGS. 50A to 50E show the sequences of several useful “bottle opener” format “skeletons”, with the Fvs of the scFv side directed to several particular anti-PD-1 ABDs, but without the Fv sequences for the “Fab” side. As will be appreciated by those in the art and outlined below, these “skeleton” sequences can be used with any Fab sequences outlined herein and contained within the sequence listing (e.g. a VH attached to the “Fab side heavy chain” or “Fab monomer” and a VL attached to the constant light chain). It should also be noted that these bottle opener skeleton sequences find use in the Central-scFv format of FIG. 1F (sometimes also referred to as the “2+1” format), with the addition of a second VH and CH1 domain as described herein. The Fab chain of each starts with a “I” delineating the beginning of the CH1 domain, such that a VH domain from an ABD as described herein is N-terminally fused to form a full length heavy chain, with the corresponding VL domain from the ABD being N-terminally fused to the “/” delineating the beginning of the CL domain in the light chain, such that a Fab is formed with the Fab chain and the light chain. The scFv chain is outlined for particular anti-PD-1 ABDs, with the CDRs underlined, the scFv linker double underlined, and “I” to indicate the junctions of domains. BO skeletons 1 to 4 (XENCS556 to 559) are identical to BO skeletons 5-8 (XENCS560 to 563) except the later include the 428L/434S “XTend®” Fc variants.

FIG. 51 shows that subject bispecific antibody XmAb20717 (anti-CTLA-4×anti-PD-1) selectively target 293 T Cells that co-express PD1 and CTLA4.

FIG. 52 shows that the binding avidity of XmAB20717 contributes to T cell activation. In particular, IFNγ levels on Day 14 are shown after human PBMCs were engrated into NSG mice on Day 0 followed by dosing with the indicated test articles on Day 1.

FIG. 53 shows that XmAB20717 promotes superior T cell activation compared to an anti-PD1 bivalent antibody. In particular, CD45+ cell counts and IFNγ levels on Day 14 are shown after human PBMCs were engrated into NSG mice on Day 0 followed by dosing with the indicated test articles on Day 1.

FIG. 54 is graphs showing that XmAb20717 enhances allogeneic anti-tumor responses in mice. NSG mice were engrafted with KG1a-luc followed by engraftment with huPBMCs. Tumor burden presented is derived from the geometric mean flux acquired by IVIS imaging of KG1a-luc.

FIG. 55 is a graph showing that PD1×CTLA4 bispecific antibodies are highly active in a mouse model for checkpoint blockade, as measured in CD45+ cell counts.

FIG. 56 is a graph showing that CTLA4×LAG3 bispecific is active and combines with anti-PD-1 for triple blockade for a mouse model for checkpoint blockade.

FIGS. 57A and 57B depict checkpoint receptor occupancy by the indicated test articles as indicated by percentage of populations of HEK293T cells expressing both CTLA-4 and PD-1 with unoccupied CTLA-4 and/or LAG-3 receptors as shown by staining.

FIG. 58 shows FACS scatter plots depicting populations of (Q1) CTLA-4-PD-1+, (Q2) CTLA-4+PD-1+, (Q3) CTLA-4-PD-1+, and (Q4) CTLA-4-PD-1-cells following treatment with the indicated test articles.

FIGS. 59A and 59B depict tumor burden (derived from the geometric mean flux acquired by IVIS imaging of KG1a-luc) in NSG mice engrafted with KG1a-luc followed by engraftment with huPBMCs following treatment with XmAb20717.

FIG. 60 depicts the binding of XmAb22841 to HEK293T cells expressing CTLA-4 and LAG-3.

FIGS. 61A to 61D depict checkpoint receptor occupancy by the indicated test articles as indicated by percentage of populations of HEK293T cells expressing both CTLA-4 and LAG-3 with unoccupied CTLA-4 and/or LAG-3 receptors as shown by staining.

FIGS. 62A and 62B show the amount of unoccupied A) LAG-3 and B) CTLA-4 receptors on HEK293T cells expressing both CTLA-4 and LAG-3 following treatment with the indicated test articles.

FIGS. 63A to 63F depict binding of the indicated test articles to SEB-stimulated T cells from 6 separate PBMC donors (A-F).

FIG. 64 depicts fold increase in IL-2 release by SEB-stimulated T cells following treatment with XENP16432, XmAb20717, XmAb22841, and XmAb22841 in combination with XENP16432 over treatment with anti-RSV mAb (XENP15074).

FIG. 65 depicts fold increase in IFNγ release by SEB-stimulated T cells following treatment with XENP16432, XmAb20717, XmAb22841, and XmAb22841 in combination with XENP16432 over treatment with anti-RSV mAb (XENP15074).

FIG. 66 depicts fold change (x-axis) in expression of immune-related genes by SEB-stimulated T cells following treatment with anti-PD-1 mAb (XENP16432) over treatment with anti-RSV mAb (XENP15074). The y-axis depicts the significance.

FIG. 67 depicts fold change (x-axis) in expression of immune-related genes by SEB-stimulated T cells following treatment with XmAb20717 over treatment with anti-RSV mAb (XENP15074).

FIG. 68 depicts fold change (x-axis) in expression of immune-related genes by SEB-stimulated T cells following treatment with XmAb22841 over treatment with anti-RSV mAb (XENP15074).

FIG. 69 depicts fold change (x-axis) in expression of immune-related genes by SEB-stimulated T cells following treatment with XmAb20717 over treatment with anti-PD-1 mAb (XENP16432).

FIG. 70 depicts fold change (x-axis) in expression of immune-related genes by SEB-stimulated T cells following treatment with XmAb22841 over treatment with anti-PD-1 mAb (XENP16432).

FIG. 71 depicts fold change (x-axis) in expression of immune-related genes by SEB-stimulated T cells following treatment with XmAb22841 in combination with anti-PD-1 mAb (XENP16432) over treatment with anti-RSV mAb (XENP15074).

FIG. 72 depicts fold change (x-axis) in expression of immune-related genes by SEB-stimulated T cells following treatment with XmAb22841 in combination with anti-PD-1 mAb (XENP16432) over treatment with anti-PD-1 mAb (XENP16432) alone.

FIG. 73 depicts the sequence for an anti-RSV antibody. It is important to note that these sequences were generated based on human IgG1, with an ablation variant (E233P/L234V/L235A/G236del/S267K, “IgG1_PVA_/S267k”). The CDRs are underlined. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on the numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems.

FIG. 74 depicts the sequences for an anti-PD-1 antibody with the variable regions from nivolumab. It is important to note that these sequences were generated based on human IgG1, with an ablation variant (E233P/L234V/L235A/G236del/S267K, “IgG1_PVA_/S267k”). The CDRs are underlined. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on the numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems.

FIG. 75 depicts the sequences for an anti-PD-1 antibody with the variable regions from pembrolizumab. It is important to note that these sequences were generated based on human IgG4, with a S228P variant. The CDRs are underlined. As noted herein and is true for every sequence herein containing CDRs, the exact identification of the CDR locations may be slightly different depending on the numbering used as is shown in Table 1, and thus included herein are not only the CDRs that are underlined but also CDRs included within the VH and VL domains using other numbering systems.

FIGS. 76A and 76B depict the pharmacokinetic profile for A) XENP20053 and B) XmAb20717 in individual mice following 2 mg/kg single i.v. administration in hFcRn (Tg276) mice.

FIG. 77 depicts the half-life of XENP20053 and XmAb20717 (individual animals) following 2 mg/kg single dose i.v. administration in hFcRn (Tg276) mice.

FIG. 78 depicts C. of XENP20053 and XmAb20717 (individual animals) following 2 mg/kg single dose i.v. administration in hFcRn (Tg276) mice.

FIG. 79 depicts the mean of selected PK parameters of XmAb20717 and XENP20053 following 2 mg/kg single dose i.v. administration in hFcRn (Tg276) mice.

FIGS. 80A to 80J depict the release of A) IFNγ, B) IL-14, C) IL-2, D) IL-4, E) IL-8, F) IL-6, G) IL-10, H) IL-12p70, I) IL-13, and J) TNFα from human PBMCs treated with PBS, plate-bound XmAb20717, soluble XmAb20717, and plate-bound anti-CD3 antibody (OKT3).

FIGS. 81A and 81B depict sensorgrams showing binding of XmAb20717 to A) human CTLA-4 and B) cynomolgus CTLA-4.

FIGS. 82A and 82B depict sensorgrams showing binding of XmAb20717 to A) human PD-1 and B) cynomolgus PD-1.

FIG. 83 depicts the equilibrium dissociation constants (K_(D)), association rates (k_(a)), and dissociation rates (k_(d)) for binding of XmAb20717 to human and cynomolgus CTLA-4 and PD-1.

FIG. 84 depicts sensorgrams from competition binding experiments of CTLA-4 and ligands CD80 and CD86 with and without XmAb20717 pre-incubation.

FIG. 85 depicts sensorgrams from competition binding experiments of PD-1 and ligands PD-L1 and PD-L2 with and without XmAb20717 pre-incubation.

FIG. 86 depicts sensorgrams showing binding of XmAb20717 (solid line) and human IgG comparator (an anti-CD19 antibody with a native IgG1 constant region; dotted line) to A) human FcγRI, B) human FcγRIIb, C) human FcγRIIA (131H), D) human FcγRIIA (131R), E) human FcγRIIIA (158V), and F) human FcγRIIIA (158F).

FIG. 87 depicts sensorgrams showing binding of XmAb20717 (solid line) and human IgG comparator (an anti-CD19 antibody with a native IgG1 constant region; dotted line) to A) cynomolgus FcγRI, B) cynomolgus FcγRIIA, C) cynomolgus FcγRIIb, and D) cynomolgus RcγRIIIA.

FIG. 88 depicts sensorgrams showing binding of XmAb20717 (solid line) and human IgG comparator (an anti-CD19 antibody with a native IgG1 constant region; dotted line) to A) murine FcγRI, B) murine FcγRIIb, C) murine FcγRIII, and D) murine FcγRIV.

FIG. 89 depicts equilibrium dissociation constants (K_(D)) for binding of XmAb20717 and XENP20053 to human, cynomolgus, and mouse FcRn at pH 6.0.

FIG. 90 depicts sensorgrams showing binding of XmAb20717 and XENP20053 to human, cynomolgus, and mouse FcRn (1000, 500, 250, and 125 nM) at pH 6.0.

FIG. 91 depicts in-tandem BLI experiment showing biosensors loaded with PD-1 and dipped into XmAb20717 or buffer followed by a final dip into CTLA-4 antigen.

FIG. 92 depicts IL-2 secretion by SEB-stimulated human PBMCs following treatment with anti-RSV mAb XENP15074, anti-PD-1 mAb XENP16432, and XmAb20717. Each point represented a unique human donor.

FIG. 93 depicts IL-2 secretion by unstimulated human PBMCs following treatment with anti-RSV mAb XENP15074, anti-PD-1 mAb XENP16432, and XmAb20717. Each point represented a unique human donor.

FIG. 94 depicts IL-2 secretion by unstimulated human PBMCs following treatment with anti-RSV mAb XENP15074, a combination of XENP20111 and XENP20059 (monovalent mAbs based on the anti-PD-1 and anti-CTLA-4 binding domains of XmAb20717), and XmAb20717. Each point represented a unique human donor.

FIG. 95 depicts changes in body weight over time (as a percentage of initial body weight) in NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles. Dead mice were set to 70% initial body weight. * denotes p<0.05, unpaired Student's t-test, each group compared to huPBMCs. Triangles indicate dosing days.

FIG. 96 depicts the survival of NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles.

FIG. 97 depicts serum IFNγ concentration over time in NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles.

FIGS. 98A to 98C depicts A) human CD45⁺ cell, B) human CD4⁺ T cell, and C) human CD8⁺ T cell counts over time in blood of NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles.

FIG. 99 depicts the sequences for XENP16434, a bivalent anti-PD-L1 mAb based on atezolizumab with an ablation variant (E233P/L234V/L235A/G236del/S267K, “IgG1_PVA_/S267k”).

FIG. 100 depicts changes in body weight over time (as a percentage of initial body weight) in NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles. Dead mice were set to 70% initial body weight.

FIG. 101 depicts the survival of NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles.

FIGS. 102A to 102C depicts A) human CD45⁺ cell, B) human CD4⁺ T cell, and C) human CD8⁺ T cell counts on Day 14 in blood of NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles.

FIG. 103 depicts the binding of XmAb20717 to PD-1⁺CTLA-4⁺ cells pretreated with the indicated concentrations of the indicated test articles.

FIG. 104 depicts the binding of XmAb20717 to PD-1⁺CTLA-4⁺ cells pretreated with the indicated concentrations of the indicated test articles.

FIG. 105 depicts the EC₅₀ of pembrolizumab for blocking XmAb20717 binding to PD-1⁺CTLA-4⁺ cells. EC₅₀ values were derived from Prism software with curve fits using a least squares method.

FIGS. 106A to 106J depict the release of A) IFNγ, B) IL-1β, C) IL-2, D) IL-4, E) IL-8, F) IL-6, G) IL-10, H) IL-12p70, I) IL-13, and J) TNFα from human PBMCs treated with PBS, plate-bound XmAb22841, soluble XmAb22841, and plate-bound anti-CD3 antibody (OKT3).

FIG. 107 depicts the sequences for XENP29154, which is in-house produced TGN1412.

FIGS. 108A to 108J depict the release of A) IFNγ, B) IL-1β, C) IL-2, D) IL-4, E) IL-8, F) IL-6, G) IL-10, H) IL-12p70, I) IL-13, and J) TNFα from human PBMCs treated with air-dried XmAb22841, air-dried XENP15074 (isotype control), and air-dried XENP29154 (positive control).

FIGS. 109A and 109B depict sensorgrams showing binding of XmAb22841 to A) human CTLA-4 and B) cynomolgus CTLA-4.

FIGS. 110A and 110B depict sensorgrams showing binding of XmAb22841 to A) human LAG-3 and B) cynomolgus LAG-3.

FIG. 111 depicts the equilibrium dissociation constants (K_(D)), association rates (k_(a)), and dissociation rates (k_(d)) for binding of XmAb22841 to human and cynomolgus CTLA-4 and LAG-3.

FIG. 112 depicts sensorgrams from competition binding experiments of CTLA-4 and ligands CD80 and CD86 with and without XmAb22841 pre-incubation.

FIG. 113 depicts blocking of soluble LAG-3-Fc binding to cell-surface MHC Class II on Ramos cells by XmAb22841.

FIG. 114 depicts sensorgrams showing binding of XmAb22841 (solid line) and human IgG comparator (an anti-CD19 antibody with a native IgG1 constant region; dotted line) to A) human FcγRI, B) human FcγRIIb, C) human FcγRIIA (131H), D) human FcγRIIA (131R), E) human FcγRIIIA (158V), and F) human FcγRIIIA (158F).

FIG. 115 depicts sensorgrams showing binding of XmAb22841 (solid line) and human IgG comparator (an anti-CD19 antibody with a native IgG1 constant region; dotted line) to A) cynomolgus FcγRI, B) cynomolgus FcγRIIA, C) cynomolgus FcγRIIb, and D) cynomolgus RcγRIIIA.

FIG. 116 depicts sensorgrams showing binding of XmAb22841 (solid line) and human IgG comparator (an anti-CD19 antibody with a native IgG1 constant region; dotted line) to A) murine FcγRI, B) murine FcγRIIb, C) murine FcγRIII, and D) murine FcγRIV.

FIG. 117 depicts equilibrium dissociation constants (K_(D)) for binding of XmAb22841 and XENP22602 to human, cynomolgus, and mouse FcRn at pH 6.0.

FIG. 118 depicts sensorgrams showing binding of XmAb22841 and XENP22602 to human, cynomolgus, and mouse FcRn (1000, 500, 250, and 125 nM) at pH 6.0.

FIG. 119 depicts in-tandem BLI experiment showing biosensors loaded with LAG-3 and dipped into XmAb22841 or buffer followed by a final dip into CTLA-4 antigen.

FIG. 120 depicts changes in body weight over time (as a percentage of initial body weight) in NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles. Dead mice were set to 70% initial body weight.

FIG. 121 depicts the survival of NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles.

FIGS. 122A and 122B depict serum A) IFNγ concentration and B) IL-10 concentrations on Days 7 and 14 in serum of NSG mice engrafted i.v. OSP with human PBMCs and dosed with the indicated test articles.

VI. DETAILED DESCRIPTION OF THE INVENTION A. Incorporation of Materials

1. Figures and Legends

All the figures, accompanying legends and sequences (with their identifiers and/or descriptions) of United States Patent Application Nos. 62/583,438, filed Nov. 8, 2017; 62/598,938, filed Dec. 14, 2017; 62/658,227, filed Apr. 16, 2018; 62/420,500, filed Nov. 10, 2016; 62/353,511, filed Jun. 22, 2016; 62/350,145, filed Jun. 14, 2016, Ser. No. 15/623,314, filed Jun. 14, 2017 and PCT/US17/37555, filed Jun. 14, 2017, all which are expressly and independently incorporated by reference herein in their entirety, particularly for the amino acid sequences depicted therein.

2. Sequences

Reference is made to the accompanying sequence listing as following: anti-PD-1 sequences suitable for use as ABDs include SEQ ID NOs: 6209-11464 (PD-1 scFv sequences, although the Fv sequences therein can be formatted as Fabs), SEQ ID NOs: 11465-17134 (PD-1 Fab sequences, although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 33003-33072 (additional PD-1 Fab sequences, although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 33073-35394 (additional PD-1 scFv sequences, although the Fv sequences therein can be formatted as Fabs) and SEQ ID NOs: 36127-36146 (PD-1 bivalent constructs, which can be formatted as either scFvs or Fabs). Anti-CTLA-4 sequences suitable for use as ABDs include SEQ ID NOs: 21-2918 (CTLA-4 scFv sequences, although the Fv sequences therein can be formatted as Fabs), SEQ ID NOs: 2919-6208 (CTLA-4 Fab sequences, although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 36739-36818 (additional CTLA-4 Fab sequences, although the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 35395-35416 (CTLA-4 one armed constructs, which can be formatted as either Fabs or scFvs). Anti-LAG-3 sequences suitable for use as ABDs include SEQ ID NOs: 17135-20764 (LAG-3 Fabs, although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 36819-36962 (additional LAG-3 Fabs although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 35417-35606 (additional LAG-3 Fabs although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 25194-32793 (additional LAG-3 Fabs although the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 32794-33002 (one armed LAG-3 constructs which can be formatted as either Fabs or scFvs). Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884 (TIM-3 Fabs, although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 37587-37698 (additional TIM-3 Fabs, the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 36347-36706 (bivalent TIM-3 constructs which can be formatted as either Fabs or scFvs). Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 (BTLA Fabs although the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 36707-36738 (additional BTLA Fabs although the Fv sequences therein can be formatted as scFvs). Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 (TIGIT Fab although the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 37435-37586 (additional TIGIT Fabs although the Fv sequences therein can be formatted as scFvs). As will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers.

Bispecific antibodies of the invention include LAG3×CTLA4 constructs of SEQ ID NOs: 35607-35866 and SEQ ID NOs: 21524-22620. PD-1×CTLA4 constructs include those listed as SEQ ID NOs: 36167-36346 and SEQ ID NOs: 23316-23735. PD-1×TIM3 constructs include those listed as SEQ ID NOs: 25174-25193. PD-1×LAG3 constructs include those listed as SEQ ID NOs: 35867-36126 and SEQ ID NOs: 23736-25133. PD-1×TIGIT constructs include those listed as SEQ ID NOs: 25134-25173. PD-1×BTLA constructs include those listed as SEQ ID NOs: 22724-23315 and SEQ ID NOs: 36147-36166. CTLA4×BTLA constructs include those listed as SEQ ID NOs: 22624-22723. Finally, the names for XENP23552, XENP22841, XENP22842, XENP22843, XENP22844, XENP22845, XENP22846, XENP22847, XENP22848, XENP22849, XENP22850, XENP22851, XENP22852, XENP22858, XENP22854, XENP22855 all should have included the “M428L/N434S” notation in the title, which were inadvertently left off.

B. Nomenclature

The bispecific antibodies of the invention are listed in several different formats. Each polypeptide is given a unique “XENP” number (or in some cases, a “XENCS” number), although as will be appreciated in the art, a longer sequence might contain a shorter one. For example, the heavy chain of the scFv side monomer of a bottle opener format for a given sequence will have a first XENP number, while the scFv domain will have a different XENP number. Some molecules have three polypeptides, so the XENP number, with the components, is used as a name. Thus, the molecule XENP20717, which is in bottle opener format, comprises three sequences, generally referred to as “XENP20717 HC-Fab”, XENP20717 HC-scFv” and “XENP20717 LC” or equivalents, although one of skill in the art would be able to identify these easily through sequence alignment. These XENP numbers are in the sequence listing as well as identifiers, and used in the Figures. In addition, one molecule, comprising the three components, gives rise to multiple sequence identifiers. For example, the listing of the Fab monomer has the full length sequence, the variable heavy sequence and the three CDRs of the variable heavy sequence; the light chain has a full length sequence, a variable light sequence and the three CDRs of the variable light sequence; and the scFv-Fc domain has a full length sequence, an scFv sequence, a variable light sequence, 3 light CDRs, a scFv linker, a variable heavy sequence and 3 heavy CDRs; note that all molecules herein with a scFv domain use a single charged scFv linker (+H), although others can be used. In addition, the naming nomenclature of particular variable domains uses a “Hx.xx_Ly.yy” type of format, with the numbers being unique identifiers to particular variable chain sequences. Thus, the variable domain of the Fab side of XENP22841 is “7G8_H3.30_11.34”, which indicates that the variable heavy domain H3.30 was combined with the light domain L1.34. In the case that these sequences are used as scFvs, the designation “7G8_H3.30_11.34”, indicates that the variable heavy domain H3.30 was combined with the light domain L1.34 and is in vh-linker-vl orientation, from N- to C-terminus. This molecule with the identical sequences of the heavy and light variable domains but in the reverse order would be named “7G8_L1.34_H3.30”. Similarly, different constructs may “mix and match” the heavy and light chains as will be evident from the sequence listing and the Figures.

C. Definitions

In order that the application may be more completely understood, several definitions are set forth below. Such definitions are meant to encompass grammatical equivalents.

By “ablation” herein is meant a decrease or removal of activity. Thus for example, “ablating FcγR binding” means the Fc region amino acid variant has less than 50% starting binding as compared to an Fc region not containing the specific variant, with more than 70-80-90-95-98% loss of activity being preferred, and in general, with the activity being below the level of detectable binding in a Biacore, SPR or BLI assay. Of particular use in the ablation of FcγR binding are those shown in FIG. 5, which generally are added to both monomers.

By “ADCC” or “antibody dependent cell-mediated cytotoxicity” as used herein is meant the cell-mediated reaction wherein nonspecific cytotoxic cells that express FcγRs recognize bound antibody on a target cell and subsequently cause lysis of the target cell. ADCC is correlated with binding to FcγRIIIa; increased binding to FcγRIIIa leads to an increase in ADCC activity.

By “ADCP” or antibody dependent cell-mediated phagocytosis as used herein is meant the cell-mediated reaction wherein nonspecific phagocytic cells that express FcγRs recognize bound antibody on a target cell and subsequently cause phagocytosis of the target cell.

By “antigen binding domain” or “ABD” herein is meant a set of six Complementary Determining Regions (CDRs) that, when present as part of a polypeptide sequence, specifically binds a target antigen as discussed herein. Thus, a “checkpoint antigen binding domain” binds a target checkpoint antigen as outlined herein. As is known in the art, these CDRs are generally present as a first set of variable heavy CDRs (vhCDRs or VHCDRs) and a second set of variable light CDRs (vlCDRs or VLCDRs), each comprising three CDRs: vhCDR1, vhCDR2, vhCDR3 for the heavy chain and vlCDR1, vlCDR2 and vlCDR3 for the light. The CDRs are present in the variable heavy and variable light domains, respectively, and together form an Fv region. (See Table 1 and related discussion above for CDR numbering schemes). Thus, in some cases, the six CDRs of the antigen binding domain are contributed by a variable heavy and a variable light domain. In a “Fab” format, the set of 6 CDRs are contributed by two different polypeptide sequences, the variable heavy domain (vh or VH; containing the vhCDR1, vhCDR2 and vhCDR3) and the variable light domain (vl or VL; containing the vlCDR1, vlCDR2 and vlCDR3), with the C-terminus of the vh domain being attached to the N-terminus of the CH1 domain of the heavy chain and the C-terminus of the vl domain being attached to the N-terminus of the constant light domain (and thus forming the light chain). In a scFv format, the vh and vl domains are covalently attached, generally through the use of a linker (a “scFv linker”) as outlined herein, into a single polypeptide sequence, which can be either (starting from the N-terminus) vh-linker-vl or vl-linker-vh, with the former being generally preferred (including optional domain linkers on each side, depending on the format used (e.g. from FIG. 1A-1O). In general, the C-terminus of the scFv domain is attached to the N-terminus of the hinge in the second monomer.

By “modification” herein is meant an amino acid substitution, insertion, and/or deletion in a polypeptide sequence or an alteration to a moiety chemically linked to a protein. For example, a modification may be an altered carbohydrate or PEG structure attached to a protein. By “amino acid modification” herein is meant an amino acid substitution, insertion, and/or deletion in a polypeptide sequence. For clarity, unless otherwise noted, the amino acid modification is always to an amino acid coded for by DNA, e.g. the 20 amino acids that have codons in DNA and RNA.

By “amino acid substitution” or “substitution” herein is meant the replacement of an amino acid at a particular position in a parent polypeptide sequence with a different amino acid. In particular, in some embodiments, the substitution is to an amino acid that is not naturally occurring at the particular position, either not naturally occurring within the organism or in any organism. For example, the substitution E272Y refers to a variant polypeptide, in this case an Fc variant, in which the glutamic acid at position 272 is replaced with tyrosine. For clarity, a protein which has been engineered to change the nucleic acid coding sequence but not change the starting amino acid (for example exchanging CGG (encoding arginine) to CGA (still encoding arginine) to increase host organism expression levels) is not an “amino acid substitution”; that is, despite the creation of a new gene encoding the same protein, if the protein has the same amino acid at the particular position that it started with, it is not an amino acid substitution.

By “amino acid insertion” or “insertion” as used herein is meant the addition of an amino acid sequence at a particular position in a parent polypeptide sequence. For example, -233E or 233E designates an insertion of glutamic acid after position 233 and before position 234. Additionally, -233ADE or A233ADE designates an insertion of AlaAspGlu after position 233 and before position 234.

By “amino acid deletion” or “deletion” as used herein is meant the removal of an amino acid sequence at a particular position in a parent polypeptide sequence. For example, E233- or E233 #, E233( ) or E233del designates a deletion of glutamic acid at position 233. Additionally, EDA233- or EDA233 # designates a deletion of the sequence GluAspAla that begins at position 233.

By “variant protein” or “protein variant”, or “variant” as used herein is meant a protein that differs from that of a parent protein by virtue of at least one amino acid modification. The protein variant has at least one amino acid modification compared to the parent protein, yet not so many that the variant protein will not align with the parental protein using an alignment program such as that described below. In general, variant proteins (such as variant Fc domains, etc., outlined herein, are generally at least 75, 80, 85, 90, 91, 92, 93, 94, 95, 96, 97, 98 or 99% identical to the parent protein, using the alignment programs described below, such as BLAST.

As described below, in some embodiments the parent polypeptide, for example an Fc parent polypeptide, is a human wild type sequence, such as the heavy constant domain or Fc region from IgG1, IgG2, IgG3 or IgG4, although human sequences with variants can also serve as “parent polypeptides”, for example the IgG1/2 hybrid of US Publication 2006/0134105 can be included. The protein variant sequence herein will preferably possess at least about 80% identity with a parent protein sequence, and most preferably at least about 90% identity, more preferably at least about 95-98-99% identity. Accordingly, by “antibody variant” or “variant antibody” as used herein is meant an antibody that differs from a parent antibody by virtue of at least one amino acid modification, “IgG variant” or “variant IgG” as used herein is meant an antibody that differs from a parent IgG (again, in many cases, from a human IgG sequence) by virtue of at least one amino acid modification, and “immunoglobulin variant” or “variant immunoglobulin” as used herein is meant an immunoglobulin sequence that differs from that of a parent immunoglobulin sequence by virtue of at least one amino acid modification. “Fc variant” or “variant Fc” as used herein is meant a protein comprising an amino acid modification in an Fc domain as compared to an Fc domain of human IgG1, IgG2 or IgG4.

The Fc variants of the present invention are defined according to the amino acid modifications that compose them. Thus, for example, N434S or 434S is an Fc variant with the substitution serine at position 434 relative to the parent Fc polypeptide, wherein the numbering is according to the EU index. Likewise, M428L/N434S defines an Fc variant with the substitutions M428L and N434S relative to the parent Fc polypeptide. The identity of the WT amino acid may be unspecified, in which case the aforementioned variant is referred to as 428L/434S. It is noted that the order in which substitutions are provided is arbitrary, that is to say that, for example, N434S/M428L is the same Fc variant as M428L/N434S, and so on. For all positions discussed in the present invention that relate to antibodies, unless otherwise noted, amino acid position numbering is according to the EU index. The EU index or EU index as in Kabat or EU numbering scheme refers to the numbering of the EU antibody. Kabat et al. collected numerous primary sequences of the variable regions of heavy chains and light chains. Based on the degree of conservation of the sequences, they classified individual primary sequences into the CDR and the framework and made a list thereof (see SEQUENCES OF IMMUNOLOGICAL INTEREST, 5th edition, NIH publication, No. 91-3242, E. A. Kabat et al., entirely incorporated by reference). See also Edelman et al., 1969, Proc Natl Acad Sci USA 63:78-85, hereby entirely incorporated by reference. The modification can be an addition, deletion, or substitution.

By “protein” herein is meant at least two covalently attached amino acids, which includes proteins, polypeptides, oligopeptides and peptides. In addition, polypeptides that make up the antibodies of the invention may include synthetic derivatization of one or more side chains or termini, glycosylation, PEGylation, circular permutation, cyclization, linkers to other molecules, fusion to proteins or protein domains, and addition of peptide tags or labels.

By “residue” as used herein is meant a position in a protein and its associated amino acid identity. For example, Asparagine 297 (also referred to as Asn297 or N297) is a residue at position 297 in the human antibody IgG1.

By “Fab” or “Fab region” as used herein is meant the polypeptide that comprises the VH, CH1, VL, and CL immunoglobulin domains, generally on two different polypeptide chains (e.g. VH-CH1 on one chain and VL-CL on the other). Fab may refer to this region in isolation, or this region in the context of a bispecific antibody of the invention. In the context of a Fab, the Fab comprises an Fv region in addition to the CH1 and CL domains.

By “Fv” or “Fv fragment” or “Fv region” as used herein is meant a polypeptide that comprises the VL and VH domains of an ABD. Fv regions can be formatted as both Fabs (as discussed above, generally two different polypeptides that also include the constant regions as outlined above) and scFvs, where the vl and vh domains are combined (generally with a linker as discussed herein) to form an scFv.

By “single chain Fv” or “scFv” herein is meant a variable heavy domain covalently attached to a variable light domain, generally using a scFv linker as discussed herein, to form a scFv or scFv domain. A scFv domain can be in either orientation from N- to C-terminus (vh-linker-vl or vl-linker-vh). In the sequences depicted in the sequence listing and in the figures, the order of the vh and vl domain is indicated in the name, e.g. H.X_L.Y means N- to C-terminal is vh-linker-vl, and L.Y_H.X is vl-linker-vh.

By “IgG subclass modification” or “isotype modification” as used herein is meant an amino acid modification that converts one amino acid of one IgG isotype to the corresponding amino acid in a different, aligned IgG isotype. For example, because IgG1 comprises a tyrosine and IgG2 a phenylalanine at EU position 296, a F296Y substitution in IgG2 is considered an IgG subclass modification.

By “non-naturally occurring modification” as used herein is meant an amino acid modification that is not isotypic. For example, because none of the human IgGs comprise a serine at position 434, the substitution 434S in IgG1, IgG2, IgG3, or IgG4 (or hybrids thereof) is considered a non-naturally occurring modification.

By “amino acid” and “amino acid identity” as used herein is meant one of the 20 naturally occurring amino acids that are coded for by DNA and RNA.

By “effector function” as used herein is meant a biochemical event that results from the interaction of an antibody Fc region with an Fc receptor or ligand. Effector functions include but are not limited to ADCC, ADCP, and CDC.

By “IgG Fc ligand” as used herein is meant a molecule, preferably a polypeptide, from any organism that binds to the Fc region of an IgG antibody to form an Fc/Fc ligand complex. Fc ligands include but are not limited to FcγRIs, FcγRIIs, FcγRIIIs, FcRn, C1q, C3, mannan binding lectin, mannose receptor, staphylococcal protein A, streptococcal protein G, and viral FcγR. Fc ligands also include Fc receptor homologs (FcRH), which are a family of Fc receptors that are homologous to the FcγRs (Davis et al., 2002, Immunological Reviews 190:123-136, entirely incorporated by reference). Fc ligands may include undiscovered molecules that bind Fc. Particular IgG Fc ligands are FcRn and Fc gamma receptors. By “Fc ligand” as used herein is meant a molecule, preferably a polypeptide, from any organism that binds to the Fc region of an antibody to form an Fc/Fc ligand complex.

By “Fc gamma receptor”, “FcγR” or “FcgammaR” as used herein is meant any member of the family of proteins that bind the IgG antibody Fc region and is encoded by an FcγR gene. In humans this family includes but is not limited to FcγRI (CD64), including isoforms FcγRIa, FcγRIb, and FcγRIc; FcγRII (CD32), including isoforms FcγRIIa (including allotypes H131 and R131), FcγRIIb (including FcγRIIb-1 and FcγRIIb-2), and FcγRIIc; and FcγRIII (CD16), including isoforms FcγRIIIa (including allotypes V158 and F158) and FcγRIIIb (including allotypes FcγRIIb-NA1 and FcγRIIb-NA2) (Jefferis et al., 2002, Immunol Lett 82:57-65, entirely incorporated by reference), as well as any undiscovered human FcγRs or FcγR isoforms or allotypes. An FcγR may be from any organism, including but not limited to humans, mice, rats, rabbits, and monkeys. Mouse FcγRs include but are not limited to FcγRI (CD64), FcγRII (CD32), FcγRIII (CD16), and FcγRIII-2 (CD16-2), as well as any undiscovered mouse FcγRs or FcγR isoforms or allotypes.

By “FcRn” or “neonatal Fc Receptor” as used herein is meant a protein that binds the IgG antibody Fc region and is encoded at least in part by an FcRn gene. The FcRn may be from any organism, including but not limited to humans, mice, rats, rabbits, and monkeys. As is known in the art, the functional FcRn protein comprises two polypeptides, often referred to as the heavy chain and light chain. The light chain is beta-2-microglobulin and the heavy chain is encoded by the FcRn gene. Unless otherwise noted herein, FcRn or an FcRn protein refers to the complex of FcRn heavy chain with beta-2-microglobulin. A variety of FcRn variants used to increase binding to the FcRn receptor, and in some cases, to increase serum half-life. An “FcRn variant” is one that increases binding to the FcRn receptor, and suitable FcRn variants are shown below.

By “parent polypeptide” as used herein is meant a starting polypeptide that is subsequently modified to generate a variant. The parent polypeptide may be a naturally occurring polypeptide, or a variant or engineered version of a naturally occurring polypeptide. Accordingly, by “parent immunoglobulin” as used herein is meant an unmodified immunoglobulin polypeptide that is modified to generate a variant, and by “parent antibody” as used herein is meant an unmodified antibody that is modified to generate a variant antibody. It should be noted that “parent antibody” includes known commercial, recombinantly produced antibodies as outlined below. In this context, a “parent Fc domain” will be relative to the recited variant; thus, a “variant human IgG1 Fc domain” is compared to the parent Fc domain of human IgG1, a “variant human IgG4 Fc domain” is compared to the parent Fc domain human IgG4, etc.

By “Fc” or “Fc region” or “Fc domain” as used herein is meant the polypeptide comprising the CH2-CH3 domains of an IgG molecule, and in some cases, inclusive of the hinge. In EU numbering for human IgG1, the CH2-CH3 domain comprises amino acids 231 to 447, and the hinge is 216 to 230. Thus the definition of “Fc domain” includes both amino acids 231-447 (CH2-CH3) or 216-447 (hinge-CH2-CH3), or fragments thereof. An “Fc fragment” in this context may contain fewer amino acids from either or both of the N- and C-termini but still retains the ability to form a dimer with another Fc domain or Fc fragment as can be detected using standard methods, generally based on size (e.g. non-denaturing chromatography, size exclusion chromatography, etc.) Human IgG Fc domains are of particular use in the present invention, and can be the Fc domain from human IgG1, IgG2 or IgG4.

A “variant Fc domain” contains amino acid modifications as compared to a parental Fc domain. Thus, a “variant human IgG1 Fc domain” is one that contains amino acid modifications (generally amino acid substitutions, although in the case of ablation variants, amino acid deletions are included) as compared to the human IgG1 Fc domain. In general, variant Fc domains have at least about 80, 85, 90, 95, 97, 98 or 99 percent identity to the corresponding parental human IgG Fc domain (using the identity algorithms discussed below, with one embodiment utilizing the BLAST algorithm as is known in the art, using default parameters). Alternatively, the variant Fc domains can have from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 amino acid modifications as compared to the parental Fc domain. Additionally, as discussed herein, the variant Fc domains herein still retain the ability to form a dimer with another Fc domain as measured using known techniques as described herein, such as non-denaturing gel electrophoresis.

By “heavy chain constant region” herein is meant the CH1-hinge-CH2-CH3 portion of an antibody (or fragments thereof), excluding the variable heavy domain; in EU numbering of human IgG1 this is amino acids 118-447 By “heavy chain constant region fragment” herein is meant a heavy chain constant region that contains fewer amino acids from either or both of the N- and C-termini but still retains the ability to form a dimer with another heavy chain constant region.

By “position” as used herein is meant a location in the sequence of a protein. Positions may be numbered sequentially, or according to an established format, for example the EU index for antibody numbering.

By “target antigen” as used herein is meant the molecule that is bound specifically by the antigen binding domain comprising the variable regions of a given antibody. As discussed below, in the present case the target antigens are checkpoint proteins.

By “strandedness” in the context of the monomers of the heterodimeric antibodies of the invention herein is meant that, similar to the two strands of DNA that “match”, heterodimerization variants are incorporated into each monomer so as to preserve the ability to “match” to form heterodimers. For example, if some pI variants are engineered into monomer A (e.g. making the pI higher) then steric variants that are “charge pairs” that can be utilized as well do not interfere with the pI variants, e.g. the charge variants that make a pI higher are put on the same “strand” or “monomer” to preserve both functionalities. Similarly, for “skew” variants that come in pairs of a set as more fully outlined below, the skilled artisan will consider pI in deciding into which strand or monomer one set of the pair will go, such that pI separation is maximized using the pI of the skews as well.

By “target cell” as used herein is meant a cell that expresses a target antigen.

By “host cell” in the context of producing a bispecific antibody according to the invention herein is meant a cell that contains the exogeneous nucleic acids encoding the components of the bispecific antibody and is capable of expressing the bispecific antibody under suitable conditions. Suitable host cells are discussed below.

By “variable region” or “variable domain” as used herein is meant the region of an immunoglobulin that comprises one or more Ig domains substantially encoded by any of the Vκ, Vλ, and/or VH genes that make up the kappa, lambda, and heavy chain immunoglobulin genetic loci respectively, and contains the CDRs that confer antigen specificity. Thus, a “variable heavy domain” pairs with a “variable light domain” to form an antigen binding domain (“ABD”). In addition, each variable domain comprises three hypervariable regions (“complementary determining regions,” “CDRs”) (vhCDR1, vhCDR2 and vhCDR3 for the variable heavy domain and vlCDR1, vlCDR2 and vlCDR3 for the variable light domain) and four framework (FR) regions, arranged from amino-terminus to carboxy-terminus in the following order: FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4.

By “wild type or WT” herein is meant an amino acid sequence or a nucleotide sequence that is found in nature, including allelic variations. A WT protein has an amino acid sequence or a nucleotide sequence that has not been intentionally modified.

The invention provides a number of antibody domains that have sequence identity to human antibody domains. Sequence identity between two similar sequences (e.g., antibody variable domains) can be measured by algorithms such as that of Smith, T. F. & Waterman, M.S. (1981) “Comparison Of Biosequences,” Adv. Appl. Math. 2:482 [local homology algorithm]; Needleman, S. B. & Wunsch, C D. (1970) “A General Method Applicable To The Search For Similarities In The Amino Acid Sequence Of Two Proteins,” J. Mol. Biol. 48:443 [homology alignment algorithm], Pearson, W. R. & Lipman, D. J. (1988) “Improved Tools For Biological Sequence Comparison,” Proc. Natl. Acad. Sci. (U.S.A.) 85:2444 [search for similarity method]; or Altschul, S. F. et al, (1990) “Basic Local Alignment Search Tool,” J. Mol. Biol. 215:403-10, the “BLAST” algorithm, see https://blast.ncbi.nlm.nih.gov/Blast/chi. When using any of the aforementioned algorithms, the default parameters (for Window length, gap penalty, etc) are used. In one embodiment, sequence identity is done using the BLAST algorithm, using default parameters

The antibodies of the present invention are generally isolated or recombinant. “Isolated,” when used to describe the various polypeptides disclosed herein, means a polypeptide that has been identified and separated and/or recovered from a cell or cell culture from which it was expressed. Ordinarily, an isolated polypeptide will be prepared by at least one purification step. An “isolated antibody,” refers to an antibody which is substantially free of other antibodies having different antigenic specificities. “Recombinant” means the antibodies are generated using recombinant nucleic acid techniques in exogeneous host cells, and they can be isolated as well.

“Specific binding” or “specifically binds to” or is “specific for” a particular antigen or an epitope means binding that is measurably different from a non-specific interaction. Specific binding can be measured, for example, by determining binding of a molecule compared to binding of a control molecule, which generally is a molecule of similar structure that does not have binding activity. For example, specific binding can be determined by competition with a control molecule that is similar to the target.

Specific binding for a particular antigen or an epitope can be exhibited, for example, by an antibody having a KD for an antigen or epitope of at least about 10⁻⁴ M, at least about 10⁻⁵ M, at least about 10⁻⁶ M, at least about 10⁻⁷M, at least about 10⁻⁸M, at least about 10⁻⁹ M, alternatively at least about 10⁻¹⁰ M, at least about 10⁻¹¹ M, at least about 10⁻¹² M, or greater, where KD refers to a dissociation rate of a particular antibody-antigen interaction. Typically, an antibody that specifically binds an antigen will have a KD that is 20-, 50-, 100-, 500-, 1000-, 5,000-, 10,000- or more times greater for a control molecule relative to the antigen or epitope.

Also, specific binding for a particular antigen or an epitope can be exhibited, for example, by an antibody having a KA or Ka for an antigen or epitope of at least 20-, 50-, 100-, 500-, 1000-, 5,000-, 10,000- or more times greater for the epitope relative to a control, where KA or Ka refers to an association rate of a particular antibody-antigen interaction. Binding affinity is generally measured using a Biacore, SPR or BLI assay.

D. Antibodies

The present invention relates to the generation of bispecific checkpoint antibodies that bind two different checkpoint antigens as discussed herein. As is discussed below, the term “antibody” is used generally. Antibodies that find use in the present invention can take on a number of formats as described herein, including traditional antibodies as well as antibody derivatives, fragments and mimetics, described herein and depicted in the figures.

Traditional antibody structural units typically comprise a tetramer. Each tetramer is typically composed of two identical pairs of polypeptide chains, each pair having one “light” (typically having a molecular weight of about 25 kDa) and one “heavy” chain (typically having a molecular weight of about 50-70 kDa). Human light chains are classified as kappa and lambda light chains. The present invention is directed to bispecific antibodies that generally are based on the IgG class, which has several subclasses, including, but not limited to IgG1, IgG2, IgG3, and IgG4. In general, IgG1, IgG2 and IgG4 are used more frequently than IgG3. It should be noted that IgG1 has different allotypes with polymorphisms at 356 (D or E) and 358 (L or M). The sequences depicted herein use the 356E/358M allotype, however the other allotype is included herein. That is, any sequence inclusive of an IgG1 Fc domain included herein can have 356D/358L replacing the 356E/358M allotype.

In addition, many of the antibodies herein have at least one of the cysteines at position 220 replaced by a serine; generally this is the on the “scFv monomer” side for most of the sequences depicted herein, although it can also be on the “Fab monomer” side, or both, to reduce disulfide formation. Specifically included within the sequences herein are one or both of these cysteines replaced (C220S).

Thus, “isotype” as used herein is meant any of the subclasses of immunoglobulins defined by the chemical and antigenic characteristics of their constant regions. It should be understood that therapeutic antibodies can also comprise hybrids of isotypes and/or subclasses. For example, as shown in US Publication 2009/0163699, incorporated by reference, the present invention the use of human IgG1/G2 hybrids.

The hypervariable region generally encompasses amino acid residues from about amino acid residues 24-34 (LCDR1; “L” denotes light chain), 50-56 (LCDR2) and 89-97 (LCDR3) in the light chain variable region and around about 31-35B (HCDR1; “H” denotes heavy chain), 50-65 (HCDR2), and 95-102 (HCDR3) in the heavy chain variable region; Kabat et al., SEQUENCES OF PROTEINS OF IMMUNOLOGICAL INTEREST, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, Md. (1991) and/or those residues forming a hypervariable loop (e.g. residues 26-32 (LCDR1), 50-52 (LCDR2) and 91-96 (LCDR3) in the light chain variable region and 26-32 (HCDR1), 53-55 (HCDR2) and 96-101 (HCDR3) in the heavy chain variable region; Chothia and Lesk (1987) J. Mol. Biol. 196:901-917. Specific CDRs of the invention are described below.

As will be appreciated by those in the art, the exact numbering and placement of the CDRs can be different among different numbering systems. However, it should be understood that the disclosure of a variable heavy and/or variable light sequence includes the disclosure of the associated (inherent) CDRs. Accordingly, the disclosure of each variable heavy region is a disclosure of the vhCDRs (e.g. vhCDR1, vhCDR2 and vhCDR3) and the disclosure of each variable light region is a disclosure of the vlCDRs (e.g. vlCDR1, vlCDR2 and vlCDR3). A useful comparison of CDR numbering is as below, see Lafranc et al., Dev. Comp. Immunol. 27(1):55-77 (2003):

TABLE 1 Kabat + Chothia IMGT Kabat AbM Chothia Contact Xencor vhCDR1 26-35  27-38 31-35 26-35 26-32 30-35  27-35 vhCDR2 50-65  56-65 50-65 50-58 52-56 47-58  54-61 vhCDR3 95-102 105-117 95-102 95-102 95-102 93-101 103-116 vlCDR1 24-34  27-38 24-34 24-34 24-34 30-36  27-38 vlCDR2 50-56  56-65 50-56 50-56 50-56 46-55  56-62 vlCDR3 89-97 105-117 89-97 89-97 89-97 89-96  97-105

Throughout the present specification, the Kabat numbering system is generally used when referring to a residue in the variable domain (approximately, residues 1-107 of the light chain variable region and residues 1-113 of the heavy chain variable region) and the EU numbering system for Fc regions (e.g, Kabat et al., supra (1991)).

Another type of Ig domain of the heavy chain is the hinge region. By “hinge” or “hinge region” or “antibody hinge region” or “hinge domain” herein is meant the flexible polypeptide comprising the amino acids between the first and second constant domains of an antibody. Structurally, the IgG CH1 domain ends at EU position 215, and the IgG CH2 domain begins at residue EU position 231. Thus for IgG the antibody hinge is herein defined to include positions 216 (E216 in IgG1) to 230 (p230 in IgG1), wherein the numbering is according to the EU index as in Kabat. In some cases, a “hinge fragment” is used, which contains fewer amino acids at either or both of the N- and C-termini of the hinge domain. As noted herein, pI variants can be made in the hinge region as well.

The light chain generally comprises two domains, the variable light domain (containing the light chain CDRs and together with the variable heavy domains forming the Fv region), and a constant light chain region (often referred to as CL or Cκ).

Another region of interest for additional substitutions, outlined herein, is the Fc region.

The present invention provides a large number of different CDR sets. In this case, a “full CDR set” comprises the three variable light and three variable heavy CDRs, e.g. a vlCDR1, vlCDR2, vlCDR3, vhCDR1, vhCDR2 and vhCDR3. These can be part of a larger variable light or variable heavy domain, respectfully. In addition, as more fully outlined herein, the variable heavy and variable light domains can be on separate polypeptide chains, when a heavy and light chain is used (for example when Fabs are used), or on a single polypeptide chain in the case of scFv sequences.

The CDRs contribute to the formation of the antigen-binding, or more specifically, epitope binding site of antibodies. “Epitope” refers to a determinant that interacts with a specific antigen binding site in the variable region of an antibody molecule known as a paratope. Epitopes are groupings of molecules such as amino acids or sugar side chains and usually have specific structural characteristics, as well as specific charge characteristics. A single antigen may have more than one epitope.

The epitope may comprise amino acid residues directly involved in the binding (also called immunodominant component of the epitope) and other amino acid residues, which are not directly involved in the binding, such as amino acid residues which are effectively blocked by the specifically antigen binding peptide; in other words, the amino acid residue is within the footprint of the specifically antigen binding peptide.

Epitopes may be either conformational or linear. A conformational epitope is produced by spatially juxtaposed amino acids from different segments of the linear polypeptide chain. A linear epitope is one produced by adjacent amino acid residues in a polypeptide chain. Conformational and nonconformational epitopes may be distinguished in that the binding to the former but not the latter is lost in the presence of denaturing solvents.

An epitope typically includes at least 3, and more usually, at least 5 or 8-10 amino acids in a unique spatial conformation. Antibodies that recognize the same epitope can be verified in a simple immunoassay showing the ability of one antibody to block the binding of another antibody to a target antigen, for example “binning.” As outlined below, the invention not only includes the enumerated antigen binding domains and antibodies herein, but those that compete for binding with the epitopes bound by the enumerated antigen binding domains.

Thus, the present invention provides different antibody domains. As described herein and known in the art, the heterodimeric antibodies of the invention comprise different domains within the heavy and light chains, which can be overlapping as well. These domains include, but are not limited to, the Fc domain, the CH1 domain, the CH2 domain, the CH3 domain, the hinge domain, the heavy constant domain (CH1-hinge-Fc domain or CH1-hinge-CH2-CH3), the variable heavy domain, the variable light domain, the light constant domain, Fab domains and scFv domains.

Thus, the “Fc domain” includes the —CH2-CH3 domain, and optionally a hinge domain (—H—CH2-CH3). For IgG, the Fc domain comprises immunoglobulin domains CH2 and CH3 (Cγ2 and Cγ3) and the lower hinge region between CH1 (Cγ1) and CH2 (Cγ2). Although the boundaries of the Fc region may vary, the human IgG heavy chain Fc region is usually defined to include residues C226 or P230 to its carboxyl-terminus, wherein the numbering is according to the EU index as in Kabat. Accordingly, “CH” domains in the context of IgG are as follows: “CH1” refers to positions 118-215 according to the EU index as in Kabat. “Hinge” refers to positions 216-230 according to the EU index as in Kabat. “CH2” refers to positions 231-340 according to the EU index as in Kabat, and “CH3” refers to positions 341-447 according to the EU index as in Kabat. Thus, the “Fc domain” includes the —CH2-CH3 domain, and optionally a hinge domain (hinge-CH2-CH3). In the embodiments herein, when a scFv is attached to an Fc domain, it is generally the C-terminus of the scFv construct that is attached to all or part of the hinge of the Fc domain; for example, it is generally attached to the sequence EPKS which is the beginning of the hinge. In some embodiments, as is more fully described below, amino acid modifications are made to the Fc region, for example to alter binding to one or more FcγR receptors or to the FcRn receptor, and to enable heterodimer formation and purification, as outlined herein.

The heavy chain comprises a variable heavy domain and a constant domain, which includes a CH1-optional hinge-Fc domain comprising a CH2-CH3. The light chain comprises a variable light chain and the light constant domain. A scFv comprises a variable heavy chain, an scFv linker, and a variable light domain. In most of the constructs and sequences outlined herein, the C-terminus of the variable heavy chain is attached to the N-terminus of the scFv linker, the C-terminus of which is attached to the N-terminus of a variable light chain (N-vh-linker-vl-C) although that can be switched (N-vl-linker-vh-C).

Some embodiments of the invention comprise at least one scFv domain, which, while not naturally occurring, generally includes a variable heavy domain and a variable light domain, linked together by a scFv linker. As outlined herein, while the scFv domain is generally from N- to C-terminus oriented as vh-scFv linker-vl, this can be reversed for any of the scFv domains (or those constructed using vh and vl sequences from Fabs), to vl-scFv linker-vh, with optional linkers at one or both ends depending on the format (see generally FIG. 1A-1O).

As shown herein, there are a number of suitable linkers (for use as either domain linkers or scFv linkers) that can be used to covalently attach the recited domains, including traditional peptide bonds, generated by recombinant techniques. In some embodiments, the linker peptide may predominantly include the following amino acid residues: Gly, Ser, Ala, or Thr. The linker peptide should have a length that is adequate to link two molecules in such a way that they assume the correct conformation relative to one another so that they retain the desired activity. In one embodiment, the linker is from about 1 to 50 amino acids in length, preferably about 1 to 30 amino acids in length. In one embodiment, linkers of 1 to 20 amino acids in length may be used, with from about 5 to about 10 amino acids finding use in some embodiments. Useful linkers include glycine-serine polymers, including for example (GS)n, (GSGGS)n (SEQ ID NO: 37756), (GGGGS)n (SEQ ID NO: 37757), and (GGGS)n (SEQ ID NO: 37758), where n is an integer of at least one (and generally from 3 to 4), glycine-alanine polymers, alanine-serine polymers, and other flexible linkers. Alternatively, a variety of nonproteinaceous polymers, including but not limited to polyethylene glycol (PEG), polypropylene glycol, polyoxyalkylenes, or copolymers of polyethylene glycol and polypropylene glycol, may find use as linkers.

Other linker sequences may include any sequence of any length of CL/CH1 domain but not all residues of CL/CH1 domain; for example the first 5-12 amino acid residues of the CL/CH1 domains. Linkers can be derived from immunoglobulin light chain, for example CK or CX. Linkers can be derived from immunoglobulin heavy chains of any isotype, including for example Cγ1, Cγ2, Cγ3, Cγ4, Cα1, Cα2, Cδ, α, and Cμ. Linker sequences may also be derived from other proteins such as Ig-like proteins (e.g. TCR, FcR, KIR), hinge region-derived sequences, and other natural sequences from other proteins.

In some embodiments, the linker is a “domain linker”, used to link any two domains as outlined herein together. For example, in FIG. 1F, there may be a domain linker that attaches the C-terminus of the CH1 domain of the Fab to the N-terminus of the scFv, with another optional domain linker attaching the C-terminus of the scFv to the CH2 domain (although in many embodiments the hinge is used as this domain linker). While any suitable linker can be used, many embodiments utilize a glycine-serine polymer as the domain linker, including for example (GS)n, (GSGGS)n (SEQ ID NO: 37756), (GGGGS)n (SEQ ID NO: 37757), and (GGGS)n (SEQ ID NO: 37758), where n is an integer of at least one (and generally from 3 to 4 to 5) as well as any peptide sequence that allows for recombinant attachment of the two domains with sufficient length and flexibility to allow each domain to retain its biological function. In some cases, and with attention being paid to “strandedness”, as outlined below, charged domain linkers, as used in some embodiments of scFv linkers can be used.

In some embodiments, the linker is a scFv linker, used to covalently attach the vh and vl domains as discussed herein. In many cases, the scFv linker is a charged scFv linker, a number of which are shown in FIGS. 7A-7B. Accordingly, the present invention further provides charged scFv linkers, to facilitate the separation in pI between a first and a second monomer. That is, by incorporating a charged scFv linker, either positive or negative (or both, in the case of scaffolds that use scFvs on different monomers), this allows the monomer comprising the charged linker to alter the pI without making further changes in the Fc domains. These charged linkers can be substituted into any scFv containing standard linkers. Again, as will be appreciated by those in the art, charged scFv linkers are used on the correct “strand” or monomer, according to the desired changes in pI. For example, as discussed herein, to make triple F format heterodimeric antibody, the original pI of the Fv region for each of the desired antigen binding domains are calculated, and one is chosen to make an scFv, and depending on the pI, either positive or negative linkers are chosen.

Charged domain linkers can also be used to increase the pI separation of the monomers of the invention as well, and thus those included in

FIGS. 7A-7B can be used in any embodiment herein where a linker is utilized.

In particular, the formats depicted in FIG. 1 are antibodies, usually referred to as “heterodimeric antibodies”, meaning that the protein has at least two associated Fc sequences self-assembled into a heterodimeric Fc domain and at least two Fv regions, whether as Fabs or as scFvs.

E. Chimeric and Humanized Antibodies

In certain embodiments, the antibodies of the invention comprise a heavy chain variable region from a particular germline heavy chain immunoglobulin gene and/or a light chain variable region from a particular germline light chain immunoglobulin gene. For example, such antibodies may comprise or consist of a human antibody comprising heavy or light chain variable regions that are “the product of” or “derived from” a particular germline sequence. A human antibody that is “the product of” or “derived from” a human germline immunoglobulin sequence can be identified as such by comparing the amino acid sequence of the human antibody to the amino acid sequences of human germline immunoglobulins and selecting the human germline immunoglobulin sequence that is closest in sequence (i.e., greatest % identity) to the sequence of the human antibody (using the methods outlined herein). A human antibody that is “the product of” or “derived from” a particular human germline immunoglobulin sequence may contain amino acid differences as compared to the germline sequence, due to, for example, naturally-occurring somatic mutations or intentional introduction of site-directed mutation. However, a humanized antibody typically is at least 90% identical in amino acids sequence to an amino acid sequence encoded by a human germline immunoglobulin gene and contains amino acid residues that identify the antibody as being derived from human sequences when compared to the germline immunoglobulin amino acid sequences of other species (e.g., murine germline sequences). In certain cases, a humanized antibody may be at least 95, 96, 97, 98 or 99%, or even at least 96%, 97%, 98%, or 99% identical in amino acid sequence to the amino acid sequence encoded by the germline immunoglobulin gene. Typically, a humanized antibody derived from a particular human germline sequence will display no more than 10-20 amino acid differences from the amino acid sequence encoded by the human germline immunoglobulin gene (prior to the introduction of any skew, pI and ablation variants herein; that is, the number of variants is generally low, prior to the introduction of the variants of the invention). In certain cases, the humanized antibody may display no more than 5, or even no more than 4, 3, 2, or 1 amino acid difference from the amino acid sequence encoded by the germline immunoglobulin gene (again, prior to the introduction of any skew, pI and ablation variants herein; that is, the number of variants is generally low, prior to the introduction of the variants of the invention).

In one embodiment, the parent antibody has been affinity matured, as is known in the art. Structure-based methods may be employed for humanization and affinity maturation, for example as described in U.S. Ser. No. 11/004,590. Selection based methods may be employed to humanize and/or affinity mature antibody variable regions, including but not limited to methods described in Wu et al., 1999, J. Mol. Biol. 294:151-162; Baca et al., 1997, J. Biol. Chem. 272(16):10678-10684; Rosok et al., 1996, J. Biol. Chem. 271(37): 22611-22618; Rader et al., 1998, Proc. Natl. Acad. Sci. USA 95: 8910-8915; Krauss et al., 2003, Protein Engineering 16(10):753-759, all entirely incorporated by reference. Other humanization methods may involve the grafting of only parts of the CDRs, including but not limited to methods described in U.S. Ser. No. 09/810,510; Tan et al., 2002, J. Immunol. 169:1119-1125; De Pascalis et al., 2002, J. Immunol. 169:3076-3084, all entirely incorporated by reference.

VII. HETERODIMERIC ANTIBODIES

Accordingly, in some embodiments the present invention provides heterodimeric checkpoint antibodies that rely on the use of two different heavy chain variant Fc sequences, that will self-assemble to form heterodimeric Fc domains and heterodimeric antibodies.

The present invention is directed to novel constructs to provide heterodimeric antibodies that allow binding to more than one checkpoint antigen or ligand, e.g. to allow for bispecific binding. The heterodimeric antibody constructs are based on the self-assembling nature of the two Fc domains of the heavy chains of antibodies, e.g. two “monomers” that assemble into a “dimer”. Heterodimeric antibodies are made by altering the amino acid sequence of each monomer as more fully discussed below. Thus, the present invention is generally directed to the creation of heterodimeric checkpoint antibodies which can co-engage antigens in several ways, relying on amino acid variants in the constant regions that are different on each chain to promote heterodimeric formation and/or allow for ease of purification of heterodimers over the homodimers.

Thus, the present invention provides bispecific antibodies. An ongoing problem in antibody technologies is the desire for “bispecific” antibodies that bind to two different antigens simultaneously, in general thus allowing the different antigens to be brought into proximity and resulting in new functionalities and new therapies. In general, these antibodies are made by including genes for each heavy and light chain into the host cells. This generally results in the formation of the desired heterodimer (A-B), as well as the two homodimers (A-A and B-B (not including the light chain heterodimeric issues)). However, a major obstacle in the formation of bispecific antibodies is the difficulty in purifying the heterodimeric antibodies away from the homodimeric antibodies and/or biasing the formation of the heterodimer over the formation of the homodimers.

There are a number of mechanisms that can be used to generate the heterodimers of the present invention. In addition, as will be appreciated by those in the art, these mechanisms can be combined to ensure high heterodimerization. Thus, amino acid variants that lead to the production of heterodimers are referred to as “heterodimerization variants”. As discussed below, heterodimerization variants can include steric variants (e.g. the “knobs and holes” or “skew” variants described below and the “charge pairs” variants described below) as well as “pI variants”, which allows purification of homodimers away from heterodimers. As is generally described in WO2014/145806, hereby incorporated by reference in its entirety and specifically as below for the discussion of “heterodimerization variants”, useful mechanisms for heterodimerization include “knobs and holes” (“KIH”; sometimes herein as “skew” variants (see discussion in WO2014/145806), “electrostatic steering” or “charge pairs” as described in WO2014/145806, pI variants as described in WO2014/145806, and general additional Fc variants as outlined in WO2014/145806 and below.

In the present invention, there are several basic mechanisms that can lead to ease of purifying heterodimeric antibodies; one relies on the use of pI variants, such that each monomer has a different pI, thus allowing the isoelectric purification of A-A, A-B and B-B dimeric proteins. Alternatively, some scaffold formats, such as the “triple F” format, also allows separation on the basis of size. As is further outlined below, it is also possible to “skew” the formation of heterodimers over homodimers. Thus, a combination of steric heterodimerization variants and pI or charge pair variants find particular use in the invention.

In general, embodiments of particular use in the present invention rely on sets of variants that include skew variants, which encourage heterodimerization formation over homodimerization formation, coupled with pI variants, which increase the pI difference between the two monomers to facilitate purification of heterodimers away from homodimers.

Additionally, as more fully outlined below, depending on the format of the heterodimer antibody, pI variants can be either contained within the constant and/or Fc domains of a monomer, or charged linkers, either domain linkers or scFv linkers, can be used. That is, scaffolds that utilize scFv(s) such as the Triple F format can include charged scFv linkers (either positive or negative), that give a further pI boost for purification purposes. As will be appreciated by those in the art, some Triple F formats are useful with just charged scFv linkers and no additional pI adjustments, although the invention does provide pI variants that are on one or both of the monomers, and/or charged domain linkers as well. In addition, additional amino acid engineering for alternative functionalities may also confer pI changes, such as Fc, FcRn and KO variants.

In the present invention that utilizes pI as a separation mechanism to allow the purification of heterodimeric proteins, amino acid variants can be introduced into one or both of the monomer polypeptides; that is, the pI of one of the monomers (referred to herein for simplicity as “monomer A”) can be engineered away from monomer B, or both monomer A and B change be changed, with the pI of monomer A increasing and the pI of monomer B decreasing. As discussed, the pI changes of either or both monomers can be done by removing or adding a charged residue (e.g. a neutral amino acid is replaced by a positively or negatively charged amino acid residue, e.g. glycine to glutamic acid), changing a charged residue from positive or negative to the opposite charge (e.g. aspartic acid to lysine) or changing a charged residue to a neutral residue (e.g. loss of a charge; lysine to serine). A number of these variants are shown in the Figures.

Accordingly, this embodiment of the present invention provides for creating a sufficient change in pI in at least one of the monomers such that heterodimers can be separated from homodimers. As will be appreciated by those in the art, and as discussed further below, this can be done by using a “wild type” heavy chain constant region and a variant region that has been engineered to either increase or decrease its pI (wt A−+B or wt A−−B), or by increasing one region and decreasing the other region (A+−B− or A−B+).

Thus, in general, a component of some embodiments of the present invention are amino acid variants in the constant regions of antibodies that are directed to altering the isoelectric point (pI) of at least one, if not both, of the monomers of a dimeric protein to form “pI antibodies” by incorporating amino acid substitutions (“pI variants” or “pI substitutions”) into one or both of the monomers. As shown herein, the separation of the heterodimers from the two homodimers can be accomplished if the pIs of the two monomers differ by as little as 0.1 pH unit, with 0.2, 0.3, 0.4 and 0.5 or greater all finding use in the present invention.

As will be appreciated by those in the art, the number of pI variants to be included on each or both monomer(s) to get good separation will depend in part on the starting pI of the components, for example in the triple F format, the starting pI of the scFv and Fab of interest. That is, to determine which monomer to engineer or in which “direction” (e.g. more positive or more negative), the Fv sequences of the two target antigens are calculated and a decision is made from there. As is known in the art, different Fvs will have different starting pIs which are exploited in the present invention. In general, as outlined herein, the pIs are engineered to result in a total pI difference of each monomer of at least about 0.1 logs, with 0.2 to 0.5 being preferred as outlined herein.

Furthermore, as will be appreciated by those in the art and outlined herein, in some embodiments, heterodimers can be separated from homodimers on the basis of size. As shown in FIG. 1A-1O for example, several of the formats allow separation of heterodimers and homodimers on the basis of size.

A. Heterodimerization Variants

The present invention provides heterodimeric proteins, including heterodimeric antibodies in a variety of formats, which utilize heterodimeric variants to allow for heterodimeric formation and/or purification away from homodimers.

There are a number of suitable pairs of sets of heterodimerization skew variants. These variants come in “pairs” of “sets”. That is, one set of the pair is incorporated into the first monomer and the other set of the pair is incorporated into the second monomer. It should be noted that these sets do not necessarily behave as “knobs in holes” variants, with a one-to-one correspondence between a residue on one monomer and a residue on the other; that is, these pairs of sets form an interface between the two monomers that encourages heterodimer formation and discourages homodimer formation, allowing the percentage of heterodimers that spontaneously form under biological conditions to be over 90%, rather than the expected 50% (25% homodimer A/A:50% heterodimer A/B:25% homodimer B/B).

B. Steric Variants

In some embodiments, the formation of heterodimers can be facilitated by the addition of steric variants. That is, by changing amino acids in each heavy chain, different heavy chains are more likely to associate to form the heterodimeric structure than to form homodimers with the same Fc amino acid sequences. Suitable steric variants are included in in the Figures.

One mechanism is generally referred to in the art as “knobs and holes”, referring to amino acid engineering that creates steric influences to favor heterodimeric formation and disfavor homodimeric formation can also optionally be used; this is sometimes referred to as “knobs and holes”, as described in U.S. Ser. No. 61/596,846, Ridgway et al., Protein Engineering 9(7):617 (1996); Atwell et al., J. Mol. Biol. 1997 270:26; U.S. Pat. No. 8,216,805, all of which are hereby incorporated by reference in their entirety. The Figures identify a number of “monomer A-monomer B” pairs that rely on “knobs and holes”. In addition, as described in Merchant et al., Nature Biotech. 16:677 (1998), these “knobs and hole” mutations can be combined with disulfide bonds to skew formation to heterodimerization.

An additional mechanism that finds use in the generation of heterodimers is sometimes referred to as “electrostatic steering” as described in Gunasekaran et al., J. Biol. Chem. 285(25):19637 (2010), hereby incorporated by reference in its entirety. This is sometimes referred to herein as “charge pairs”. In this embodiment, electrostatics are used to skew the formation towards heterodimerization. As those in the art will appreciate, these may also have an effect on pI, and thus on purification, and thus could in some cases also be considered pI variants. However, as these were generated to force heterodimerization and were not used as purification tools, they are classified as “steric variants”. These include, but are not limited to, D221E/P228E/L368E paired with D221R/P228R/K409R (e.g. these are “monomer corresponding sets) and C220E/P228E/368E paired with C220R/E224R/P228R/K409R.

Additional monomer A and monomer B variants that can be combined with other variants, optionally and independently in any amount, such as pI variants outlined herein or other steric variants that are shown in FIG. 37 of US 2012/0149876, the figure and legend and SEQ ID NOs of which are incorporated expressly by reference herein.

In some embodiments, the steric variants outlined herein can be optionally and independently incorporated with any pI variant (or other variants such as Fc variants, FcRn variants, etc.) into one or both monomers, and can be independently and optionally included or excluded from the proteins of the invention.

A list of suitable skew variants is found in FIG. 3A-3F and FIG. 8 showing some pairs of particular utility in many embodiments. Of particular use in many embodiments are the pairs of sets including, but not limited to, S364K/E357Q: L368D/K370S; L368D/K370S: S364K; L368E/K370S: S364K; T411T/E360E/Q362E: D401K; L368D/K370S: S364K/E357L, K370S: S364K/E357Q and T366S/L368A/Y407V: T366W (optionally including a bridging disulfide, T366S/L368A/Y407V/Y349C: T366W/S354C). In terms of nomenclature, the pair “S364K/E357Q: L368D/K370S” means that one of the monomers has the double variant set S364K/E357Q and the other has the double variant set L368D/K370S; as above, the “strandedness” of these pairs depends on the starting pI.

C. pI (Isoelectric Point) Variants for Heterodimers

In general, as will be appreciated by those in the art, there are two general categories of pI variants: those that increase the pI of the protein (basic changes) and those that decrease the pI of the protein (acidic changes). As described herein, all combinations of these variants can be done: one monomer may be wild type, or a variant that does not display a significantly different pI from wild-type, and the other can be either more basic or more acidic. Alternatively, each monomer is changed, one to more basic and one to more acidic.

Preferred combinations of pI variants are shown in FIG. 4. As outlined herein and shown in the figures, these changes are shown relative to IgG1, but all isotypes can be altered this way, as well as isotype hybrids. In the case where the heavy chain constant domain is from IgG2-4, R133E and R133Q can also be used.

In one embodiment, for example in the FIG. 1A, E, F, G, H and I formats, a preferred combination of pI variants has one monomer (the negative Fab side) comprising 208D/295E/384D/418E/421D variants (N208D/Q295E/N384D/Q418E/N421D when relative to human IgG1) and a second monomer (the positive scFv side) comprising a positively charged scFv linker, including (GKPGS)4 (SEQ ID NO: 37755). However, as will be appreciated by those in the art, the first monomer includes a CH1 domain, including position 208. Accordingly, in constructs that do not include a CH1 domain (for example for antibodies that do not utilize a CH1 domain on one of the domains, for example in a dual scFv format or a “one armed” format such as those depicted in FIG. 1B, C or D), a preferred negative pI variant Fc set includes 295E/384D/418E/421D variants (Q295E/N384D/Q418E/N421D when relative to human IgG1).

Accordingly, in some embodiments, one monomer has a set of substitutions from FIG. 4 and the other monomer has a charged linker (either in the form of a charged scFv linker because that monomer comprises an scFv or a charged domain linker, as the format dictates, which can be selected from those depicted in FIGS. 7A-7B).

1. Isotypic Variants

In addition, many embodiments of the invention rely on the “importation” of pI amino acids at particular positions from one IgG isotype into another, thus reducing or eliminating the possibility of unwanted immunogenicity being introduced into the variants. A number of these are shown in FIG. 21 of US Publ. 2014/0370013, hereby incorporated by reference. That is, IgG1 is a common isotype for therapeutic antibodies for a variety of reasons, including high effector function. However, the heavy constant region of IgG1 has a higher pI than that of IgG2 (8.10 versus 7.31). By introducing IgG2 residues at particular positions into the IgG1 backbone, the pI of the resulting monomer is lowered (or increased) and additionally exhibits longer serum half-life. For example, IgG1 has a glycine (pI 5.97) at position 137, and IgG2 has a glutamic acid (pI 3.22); importing the glutamic acid will affect the pI of the resulting protein. As is described below, a number of amino acid substitutions are generally required to significant affect the pI of the variant antibody. However, it should be noted as discussed below that even changes in IgG2 molecules allow for increased serum half-life.

In other embodiments, non-isotypic amino acid changes are made, either to reduce the overall charge state of the resulting protein (e.g. by changing a higher pI amino acid to a lower pI amino acid), or to allow accommodations in structure for stability, etc. as is more further described below.

In addition, by pI engineering both the heavy and light constant domains, significant changes in each monomer of the heterodimer can be seen. As discussed herein, having the pIs of the two monomers differ by at least 0.5 can allow separation by ion exchange chromatography or isoelectric focusing, or other methods sensitive to isoelectric point.

D. Calculating pI

The pI of each monomer can depend on the pI of the variant heavy chain constant domain and the pI of the total monomer, including the variant heavy chain constant domain and the fusion partner. Thus, in some embodiments, the change in pI is calculated on the basis of the variant heavy chain constant domain, using the chart in the FIG. 19 of US Pub. 2014/0370013. As discussed herein, which monomer to engineer is generally decided by the inherent pI of the Fv and scaffold regions. Alternatively, the pI of each monomer can be compared.

E. pI Variants that Also Confer Better FcRn In Vivo Binding

In the case where the pI variant decreases the pI of the monomer, they can have the added benefit of improving serum retention in vivo.

Although still under examination, Fc regions are believed to have longer half-lives in vivo, because binding to FcRn at pH 6 in an endosome sequesters the Fc (Ghetie and Ward, 1997 Immunol Today. 18(12): 592-598, entirely incorporated by reference). The endosomal compartment then recycles the Fc to the cell surface. Once the compartment opens to the extracellular space, the higher pH, ˜7.4, induces the release of Fc back into the blood. In mice, Dall'Acqua et al. showed that Fc mutants with increased FcRn binding at pH 6 and pH 7.4 actually had reduced serum concentrations and the same half life as wild-type Fc (Dail' Acqua et al. 2002, J. Immunol. 169:5171-5180, entirely incorporated by reference). The increased affinity of Fc for FcRn at pH 7.4 is thought to forbid the release of the Fc back into the blood. Therefore, the Fc mutations that will increase Fc's half-life in vivo will ideally increase FcRn binding at the lower pH while still allowing release of Fc at higher pH. The amino acid histidine changes its charge state in the pH range of 6.0 to 7.4. Therefore, it is not surprising to find His residues at important positions in the Fc/FcRn complex.

Recently it has been suggested that antibodies with variable regions that have lower isoelectric points may also have longer serum half-lives (Igawa et al., 2010 PEDS. 23(5): 385-392, entirely incorporated by reference). However, the mechanism of this is still poorly understood. Moreover, variable regions differ from antibody to antibody. Constant region variants with reduced pI and extended half-life would provide a more modular approach to improving the pharmacokinetic properties of antibodies, as described herein.

F. Additional Fc Variants for Additional Functionality

In addition to pI amino acid variants, there are a number of useful Fc amino acid modification that can be made for a variety of reasons, including, but not limited to, altering binding to one or more FcγR receptors, altered binding to FcRn receptors, etc.

Accordingly, the proteins of the invention can include amino acid modifications, including the heterodimerization variants outlined herein, which includes the pI variants and steric variants. Each set of variants can be independently and optionally included or excluded from any particular heterodimeric protein.

G. FcγR Variants

Accordingly, there are a number of useful Fc substitutions that can be made to alter binding to one or more of the FcγR receptors. Substitutions that result in increased binding as well as decreased binding can be useful. For example, it is known that increased binding to FcγRIIIa results in increased ADCC (antibody dependent cell-mediated cytotoxicity; the cell-mediated reaction wherein nonspecific cytotoxic cells that express FcγRs recognize bound antibody on a target cell and subsequently cause lysis of the target cell). Similarly, decreased binding to FcγRIIb (an inhibitory receptor) can be beneficial as well in some circumstances. Amino acid substitutions that find use in the present invention include those listed in U.S. Ser. No. 11/124,620 (particularly FIG. 41), Ser. Nos. 11/174,287, 11/396,495, 11/538,406, all of which are expressly incorporated herein by reference in their entirety and specifically for the variants disclosed therein. Particular variants that find use include, but are not limited to, 236A, 239D, 239E, 332E, 332D, 239D/332E, 267D, 267E, 328F, 267E/328F, 236A/332E, 239D/332E/330Y, 239D, 332E/330L, 243A, 243L, 264A, 264V and 299T.

In addition, there are additional Fc substitutions that find use in increased binding to the FcRn receptor and increased serum half life, as specifically disclosed in U.S. Ser. No. 12/341,769, hereby incorporated by reference in its entirety, including, but not limited to, 434S, 434A, 428L, 308F, 259I, 428L/434S, 259I/308F, 436I/428L, 436I or V/434S, 436V/428L and 259I/308F/428L.

H. Ablation Variants

Similarly, another category of functional variants are “FcγR ablation variants” or “Fc knock out (FcKO or KO)” variants. In these embodiments, for some therapeutic applications, it is desirable to reduce or remove the normal binding of the Fc domain to one or more or all of the Fcγ receptors (e.g. FcγR1, FcγRIIa, FcγRIIb, FcγRIIIa, etc.) to avoid additional mechanisms of action. That is, for example, in many embodiments, particularly in the use of bispecific checkpoint antibodies desirable to ablate FcγRIIIa binding to eliminate or significantly reduce ADCC activity such that one of the Fc domains comprises one or more Fcγ receptor ablation variants. These ablation variants are depicted in FIG. 5, and each can be independently and optionally included or excluded, with preferred aspects utilizing ablation variants selected from the group consisting of G236R/L328R, E233P/L234V/L235A/G236del/S239K, E233P/L234V/L235A/G236del/S267K, E233P/L234V/L235A/G236del/S239K/A327G, E233P/L234V/L235A/G236del/S267K/A327G and E233P/L234V/L235A/G236del. It should be noted that the ablation variants referenced herein ablate FcγR binding but generally not FcRn binding.

As is known in the art, the Fc domain of human IgG1 has the highest binding to the Fcγ receptors, and thus ablation variants can be used when the constant domain (or Fc domain) in the backbone of the heterodimeric antibody is IgG1. Alternatively, or in addition to ablation variants in an IgG1 background, mutations at the glycosylation position 297 (generally to A or S) can significantly ablate binding to FcγRIIIa, for example. Human IgG2 and IgG4 have naturally reduced binding to the Fcγ receptors, and thus those backbones can be used with or without the ablation variants.

I. Combination of Heterodimeric and Fc Variants

As will be appreciated by those in the art, all of the recited heterodimerization variants (including skew and/or pI variants) can be optionally and independently combined in any way, as long as they retain their “strandedness” or “monomer partition”. In addition, all of these variants can be combined into any of the heterodimerization formats.

In the case of pI variants, while embodiments finding particular use are shown in the Figures, other combinations can be generated, following the basic rule of altering the pI difference between two monomers to facilitate purification.

In addition, any of the heterodimerization variants, skew and pI, are also independently and optionally combined with Fc ablation variants, Fc variants, FcRn variants, as generally outlined herein. Preferred combinations are shown in FIGS. 6A-6B.

Antigen Binding Domains to Target Antigens

The bispecific antibodies of the invention have two different antigen binding domains (ABDs) that bind to two different target antigens (“target pairs”), in either bivalent, bispecific formats or trivalent, bispecific formats as generally shown in FIG. 1A-1O. In the present invention, the bispecific heterodimeric antibodies target human PD-1 on one side and a second antigen on the other side selected from CTLA-4, TIM-3, LAG-3, TIGIT, ICOS and BTLA, the sequences of which are shown in FIG. 2. Accordingly, suitable bispecific antibodies bind PD-1 and CTLA-4, PD-1 and TIM-3, PD-1 and LAG-3, PD-1 and TIGIT, PD-1 and BTLA and PD-1 and ICOS. Note that generally these bispecific antibodies are named “anti-PD-1×anti-CTLA-4”, or generally simplistically or for ease (and thus interchangeably) as “PD-1×CTLA-4”, etc. for each pair. Note that unless specified herein, the order of the antigen list in the name does not confer structure; that is a PD-1×CTLA-4 bottle opener antibody can have the scFv bind to PD-1 or CTLA-4, although in some cases, the order specifies structure as indicated.

As is more fully outlined herein, these combinations of ABDs can be in a variety of formats, as outlined below, generally in combinations where one ABD is in a Fab format and the other is in an scFv format. As discussed herein and shown in FIG. 1A-1O, some formats use a single Fab and a single scFv (FIG. 1A, C and D), and some formats use two Fabs and a single scFv (FIG. 1E, F, G, H and I).

VIII. ANTIGEN BINDING DOMAINS

As discussed herein, the bispecific heterodimeric antibodies of the invention include two antigen binding domains (ABDs), each of which bind to a different target protein. As outlined herein, these heterodimeric antibodies can be bispecific and bivalent (each antigen is bound by a single ABD, for example, in the format depicted in FIG. 1A), or bispecific and trivalent (one antigen is bound by a single ABD and the other is bound by two ABDs, for example as depicted in FIG. 1F).

In addition, in general, one of the ABDs comprises a scFv as outlined herein, in an orientation from N- to C-terminus of vh-scFv linker-vl or vl-scFv linker-vh. One or both of the other ABDs, according to the format, generally is a Fab, comprising a vh domain on one protein chain (generally as a component of a heavy chain) and a vl on another protein chain (generally as a component of a light chain).

The invention provides a number of ABDs that bind to a number of different target proteins, as outlined below. As will be appreciated by those in the art, any set of 6 CDRs or vh and vl domains can be in the scFv format or in the Fab format, which is then added to the heavy and light constant domains, where the heavy constant domains comprise variants (including within the CH1 domain as well as the Fc domain). The scFv sequences contained in the sequence listing utilize a particular charged linker, but as outlined herein, uncharged or other charged linkers can be used, including those depicted in FIGS. 7A-7B.

In addition, as discussed above, the numbering used in the Sequence Listing for the identification of the CDRs is Kabat, however, different numbering can be used, which will change the amino acid sequences of the CDRs as shown in Table 1.

For all of the variable heavy and light domains listed herein, further variants can be made. As outlined herein, in some embodiments the set of 6 CDRs can have from 0, 1, 2, 3, 4 or 5 amino acid modifications (with amino acid substitutions finding particular use), as well as changes in the framework regions of the variable heavy and light domains, as long as the frameworks (excluding the CDRs) retain at least about 80, 85 or 90% identity to a human germline sequence selected from those listed in FIG. 1 of U.S. Pat. No. 7,657,380, which Figure and Legend is incorporated by reference in its entirety herein. Thus, for example, the identical CDRs as described herein can be combined with different framework sequences from human germline sequences, as long as the framework regions retain at least 80, 85 or 90% identity to a human germline sequence selected from those listed in FIG. 1 of U.S. Pat. No. 7,657,380. Alternatively, the CDRs can have amino acid modifications (e.g. from 1, 2, 3, 4 or 5 amino acid modifications in the set of CDRs (that is, the CDRs can be modified as long as the total number of changes in the set of 6 CDRs is less than 6 amino acid modifications, with any combination of CDRs being changed; e.g. there may be one change in vlCDR1, two in vhCDR2, none in vhCDR3, etc.)), as well as having framework region changes, as long as the framework regions retain at least 80, 85 or 90% identity to a human germline sequence selected from those listed in FIG. 1 of U.S. Pat. No. 7,657,380.

A. PD-1 Antigen Binding Domains

In the embodiments of the invention, one of the ABDs binds human PD-1. WO 2017/218707, hereby expressly incorporated by reference in its entirety, and specifically for Figures, Legends and SEQ identifiers that depict anti-PD-1 sequences, outlines a large number of anti-PD-1 ABDs, that can be used in combination with ABDs to other checkpoint inhibitors. However, the present disclosure is directed to additional anti-PD-1 ABDs based on the 1C11 clone, shown in FIGS. 13, 15, 16, 18, 20, 21, 24, 33 and 40.

As is known in the art, stability of variable domains can change based on the format. That is, VH and VL domains that are identified and/or useful in a Fab format may not be as stable in an scFv format, and thus sometimes additional engineering occurs to increase stability (e.g. Tm).

In useful embodiments, the invention provides anti-PD-1 ABDs comprising a VHCDR1 comprising the amino acid sequence HYG(M/I)N; a VHCDR2 comprising the amino acid sequence WINT(Y/H)TGEP(T/Y)YA(D/P)GF(T/Q)(G/E); a VHCDR3 comprising the amino acid sequence DY(F/Y)GSSPY; a VLCDR1 comprising the amino acid sequence VLCDR1 R(S/A)SQSIV(F/H)SNGNTYLE; a VLCDR2 comprising the amino acid sequence KVSNRF(S/T); and a VHCDR3 comprising the amino acid sequence FQGSHVPN. As is known, amino acids depicted as “(S/T)” means that either amino acid can be at this position.

In useful embodiments, the bispecific antibodies of the invention include an ABD to human PD-1. In these embodiments, the six CDRs that confer binding to PD-1 are selected from those depicted in any of FIGS. 13, 15, 16, 18, 20, 21, 24, 33 and 40. Alternatively in these embodiments, the VH and VL domains that confer binding to PD-1 are selected from those depicted in any of FIGS. 13, 15, 16, 18, 20, 21, 24, 33 and 40.

In some embodiments, the bispecific antibodies of the invention include an ABD to PD-1 in a Fab format. In some embodiments, the ABD to PD-1 contains the 6 CDRs of any ABDs of FIGS. 13, 16, 18, 20, 21, 24, 33 and 40, or the VH and VL domains from any ABD of FIGS. 13, 16, 18, 20, 21, 24, 33 and 40.

Of particular use in many embodiments that have a Fab ABD to PD-1 is the ABD of XENP26940 1C11[PD-1]_H3.303_L3.152 of FIGS. 24A-24J. Thus, the six CDRs and/or the VH and VL domains from XENP026940 can be used in the constructs of the invention.

Of particular use in many embodiments that have a Fab ABD to PD-1 is the ABD of XENP28652 1C11[PD-1]_H3.328_L3.153 of FIG. 40. Thus, the six CDRs and/or the VH and VL domains from XENP28652 can be used in the constructs of the invention.

In some embodiments, the bispecific antibodies of the invention include an ABD to PD-1 in a scFv format. In some embodiments, the ABD to PD-1 contains the 6 CDRs of any ABDs of FIG. 15A-15T, or the VH and VL domains from any ABD of FIG. 15A-15T.

Of particular use in many embodiments that have a scFv ABD to PD-1 is the ABD of XENP025806 1C11[PD-1]_H3.234_L3.144 as depicted in FIG. 15A-15T. Thus, the six CDRs and/or the VH and VL domains from XENP025806 can be used in the constructs of the invention.

Of particular use in many embodiments that have a scFv ABD to PD-1 is the ABD of XENP025812 1C11[PD-1]_H3.240_L3.148 as depicted in FIG. 15A-15T. Thus, the six CDRs and/or the VH and VL domains from XENP025812 can be used in the constructs of the invention.

Of particular use in many embodiments that have a scFv ABD to PD-1 is the ABD of XENP025813 1C11[PD-1]_H3.241_L3.148 as depicted in FIG. 15A-15T. Thus, the six CDRs and/or the VH and VL domains from XENP025813 can be used in the constructs of the invention.

Of particular use in many embodiments that have a scFv ABD to PD-1 is the ABD of XENP025819 1C11[PD-1]_H3.241_L3.92 as depicted in FIG. 15A-15T. Thus, the six CDRs and/or the VH and VL domains from XENP025819 can be used in the constructs of the invention.

B. CTLA-4 Antigen Binding Domains

As will be appreciated by those in the art, any number of anti-CTLA-4 ABD sequences can be used in combination with the scFv anti-PD-1 sequences of the invention in the creation of bispecific antibodies. Anti-CTLA-4 sequences suitable for use as ABDs include SEQ ID NOs: 21-2918 (CTLA-4 scFv sequences, although the Fv sequences therein can be formatted as Fabs), SEQ ID NOs: 2919-6208 (CTLA-4 Fab sequences, although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 36739-36818 (additional CTLA-4 Fab sequences, although the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 35395-35416 (CTLA-4 one armed constructs, which can be formatted as either Fabs or scFvs). As will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers.

In some embodiments, an anti-CTLA-4 Fab is selected from the pairs of SEQ ID NOs:36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807 and 36811 and 36815 of the sequence listing.

Of particular interest in the present invention are the sequences of the Fab CTLA-4 ABD of CTLA-4 H3_L0.22, including the VH (SEQ ID NO:38134, with VHCDRs (SEQ ID NOs:38135, 38136 and 38137) and VL (SEQ ID NO:38138 with VLCDRs (SEQ ID NOs:38139, 38140 and 38141).

C. LAG-3 Antigen Binding Domains

As will be appreciated by those in the art, any number of anti-LAG-3 ABD sequences can be used in combination with the scFv anti-PD-1 sequences of the invention in the creation of bispecific antibodies. Anti-LAG-3 sequences suitable for use as ABDs include SEQ ID NOs: 17135-20764 (LAG-3 Fabs, although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 36819-36962 (additional LAG-3 Fabs although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 35417-35606 (additional LAG-3 Fabs although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 25194-32793 (additional LAG-3 Fabs although the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 32794-33002 (one armed LAG-3 constructs which can be formatted as either Fabs or scFvs). As will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers.

In some embodiments, an anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959.

Of particular interest in the present invention are the sequences of the LAG-3 Fab ABD of XENP22594, including the VH (SEQ ID NO:32755, with VHCDRs (SEQ ID NOs:32756, 32757 and 32758) and VL (SEQ ID NO:32760 with VLCDRs (SEQ ID NOs:32761, 32762 and 32763).

Of particular interest in the present invention are the sequences of the LAG-3 Fab ABD of XENP22656, including the VH (SEQ ID NO:28815, with VHCDRs (SEQ ID NOs:28816, 28817, and 28118) and VL (SEQ ID NO:28820, with VLCDRs (SEQ ID NOs:28821, 28822 and 28823).

D. TIM-3 Antigen Binding Domains

As will be appreciated by those in the art, any number of anti-TIM-3 ABD sequences can be used in combination with the scFv anti-PD-1 sequences of the invention in the creation of bispecific antibodies. Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884 (TIM-3 Fabs, although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 37587-37698 (additional TIM-3 Fabs, the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 36347-36706 (bivalent TIM-3 constructs which can be formatted as either Fabs or scFvs). As will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers.

In some embodiments, the anti-TIM-3 ABD is selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695.

Of particular interest in the present invention are the Fab sequences of the anti-TIM-3 ABD of XENP21189, including the VH (SEQ ID NO:36508, with VHCDRs (SEQ ID NOs:36509, 36510 and 36511) and VL (SEQ ID NO:36513, with VLCDRs (SEQ ID NOs:36514, 36515 and 36516).

E. BTLA Antigen Binding Domains

As will be appreciated by those in the art, any number of anti-BTLA ABD sequences can be used in combination with the scFv anti-PD-1 sequences of the invention in the creation of bispecific antibodies. Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 (BTLA Fabs although the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 36707-36738 (additional BTLA Fabs although the Fv sequences therein can be formatted as scFvs). As will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers.

In some embodiments, the anti-BTLA ABD of use in the invention are selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735.

Of particular interest in the present invention are the Fab sequences of the anti-BTLA ABD of XENP20269, including the VH (SEQ ID NO:20936, with VHCDRs (SEQ ID NOs:20937, 20938 and 20939) and VL (SEQ ID NO:20941, with VLCDRs (SEQ ID NOs:20942, 20943 and 20944).

F. ICOS Antigen Binding Domains

As will be appreciated by those in the art, any number of anti-ICOS ABD sequences can be used in combination with the scFv anti-PD-1 sequences of the invention in the creation of bispecific antibodies. Anti-ICOS sequences suitable for use as ABDs include many as disclosed in US2018/0127501, expressly incorporated by reference in its entirety and specifically for the legends and FIGS. 19, 20 and 24, the sequences depicted therein, as well as SEQ ID NOs:27869-28086 from US2018/0127501 which contain a number of ICOS Fab sequences (heavy chain VH1-CH1 and light chain VL1-CL) as indicated in the naming nomenclature. As will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers.

In some embodiments, the anti-ICOS ABD of use in the invention are selected from the pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501.

Of particular interest in the present invention are the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK, with VH_ICOS_H0_L0 and VL_ICOS_H0_L0.

Of particular interest in the present invention are the Fab sequences of the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK, with VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0.

G. TIGIT Antigen Binding Domains

Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583.

IX. MONOVALENT ANTI-PD-1 ANTIBODIES

In addition, as will be appreciated by those in the art, the novel Fv sequences outlined herein can also be used in both monospecific antibodies (e.g. “traditional monoclonal antibodies”) or non-heterodimeric bispecific formats.

Accordingly, the present invention provides monoclonal (monospecific) antibodies comprising the 6 CDRs and/or the vh and vl sequences from the figures, generally with IgG1, IgG2, IgG3 or IgG4 constant regions, with IgG1, IgG2 and IgG4 (including IgG4 constant regions comprising a S228P amino acid substitution) finding particular use in some embodiments. That is, any sequence herein with a “H_L” designation can be linked to the constant region of a human IgG1 antibody.

A. Anti-PD-1 Monoclonal Antibodies

As will be appreciated by those in the art, the novel Fv sequences outlined herein can also be used in both monospecific antibodies (e.g. “traditional monoclonal antibodies”) or non-heterodimeric bispecific formats. Accordingly, the present invention provides monoclonal (monospecific) antibodies comprising the 6 CDRs and/or the vh and vl sequences from the figures, generally with IgG1, IgG2, IgG3 or IgG4 constant regions, with IgG1, IgG2 and IgG4 (including IgG4 constant regions comprising a S228P amino acid substitution) finding particular use in some embodiments. That is, any sequence herein with a “H_L” designation can be linked to the constant region of a human IgG1 antibody.

In some embodiments, the monoclonal antibody is selected from those depicted in FIGS. 13, 16, 18, 20, 21, 24, 33 and 40.

In some embodiments, antibodies comprising a VH and VL domain from XENP26940 1C11[PD-1]_H3.303_L3.152 of FIGS. 24A-24J. Thus, the six CDRs and/or the VH and VL domains from XENP026940 can be used in the creation of monoclonal antibodies. In some embodiments, the VH and VL from XENP026940 can be used with a IgG1 constant domain. In some embodiments, the VH and VL from XENP026940 can be used with a IgG1 constant domain, that may contain additional Fc variants, in particular the 428L/434S FcRn variants. In some embodiments, the VH and VL from XENP026940 can be used with a IgG4 constant domain, particularly with a S228P amino acid substitution. In some embodiments, the antibody is XENP26940.

In some embodiments, antibodies comprising a VH and VL domain from XENP28652 1C11[PD-1]_H3.328_L3.153 of FIG. 40. Thus, the six CDRs and/or the VH and VL domains from XENP28652 can be used in the creation of monoclonal antibodies. In some embodiments, the VH and VL from XENP28652 can be used with a IgG1 constant domain. In some embodiments, the VH and VL from XENP28652 can be used with a IgG1 constant domain, that may contain additional Fc variants, in particular the 428L/434S FcRn variants. In some embodiments, the VH and VL from XENP28652 can be used with a IgG4 constant domain, particularly with a S228P amino acid substitution. In some embodiments, the antibody is XENP28652.

X. USEFUL FORMATS OF THE INVENTION

As will be appreciated by those in the art and discussed more fully below, the bispecific heterodimeric antibodies of the present invention can take on a wide variety of configurations, as are generally depicted in FIG. 1. Some figures depict “single ended” configurations, where there is one type of specificity on one “arm” of the molecule and a different specificity on the other “arm”. Other figures depict “dual ended” configurations, where there is at least one type of specificity at the “top” of the molecule and one or more different specificities at the “bottom” of the molecule. Thus, the present invention is directed to novel immunoglobulin compositions that co-engage a different first and a second antigen.

As will be appreciated by those in the art, the heterodimeric formats of the invention can have different valencies as well as be bispecific. That is, heterodimeric antibodies of the invention can be bivalent and bispecific, wherein one checkpoint target is bound by one ABD and the other checkpoint target is bound by a second ABD. The heterodimeric antibodies can also be trivalent and bispecific, wherein the first antigen is bound by two ABDs and the second antigen by a second ABD.

A. Bottle Opener Format

One heterodimeric scaffold that finds particular use in the present invention is the “triple F” or “bottle opener” scaffold format as shown in FIG. 1. In this embodiment, one heavy chain of the antibody contains a single chain Fv (“scFv”, as defined herein) and the other heavy chain is a “regular” Fab format, comprising a variable heavy chain and a light chain. This structure is sometimes referred to herein as “triple F” format (scFv-Fab-Fc) or the “bottle-opener” (BO) format, due to a rough visual similarity to a bottle-opener (see FIG. 1A). The two chains are brought together by the use of amino acid variants in the constant regions (e.g. the Fc domain, the CH1 domain and/or the hinge region) that promote the formation of heterodimeric antibodies as is described more fully below.

There are several distinct advantages to the present “triple F” format. As is known in the art, antibody analogs relying on two scFv constructs often have stability and aggregation problems, which can be alleviated in the present invention by the addition of a “regular” heavy and light chain pairing. In addition, as opposed to formats that rely on two heavy chains and two light chains, there is no issue with the incorrect pairing of heavy and light chains (e.g. heavy 1 pairing with light 2, etc.).

Many of the embodiments outlined herein rely in general on the bottle opener format that comprises a first monomer comprising an scFv (sometimes referred to herein as the “scFv monomer” or “scFv chain” of the BO format), comprising a variable heavy and a variable light domain, covalently attached using an scFv linker (charged, in many but not all instances), where the scFv is covalently attached to the N-terminus of a first Fc domain usually through a domain linker (which, as outlined herein can either be un-charged or charged and can be exogeneous or endogeneous (e.g. all or part of the native hinge domain). Thus the scFv monomer can have, from N-terminal to C-terminal, a structure selected from VH1-scFv linker-VII-optional linker-CH2-CH3, VL1-scFv linker-VH1-optional linker-CH2-CH3, VH1-scFv linker-VL1-hinge-CH2-CH3 and VL1-scFv linker-VH1-hinge-CH2-CH3. The second monomer of the bottle opener format is a heavy chain (VH2-CH1-hinge-CH2-CH3), and the composition further comprises a light chain (VL2-CL).

In addition, the Fc domains of the bottle opener format generally comprise skew variants (e.g. a set of amino acid substitutions as shown in FIG. 3A-3F and FIG. 8, with particularly useful skew variants being selected from the group consisting of S364K/E357Q: L368D/K370S; L368D/K370S: S364K; L368E/K370S: S364K; T411T/E360E/Q362E: D401K; L368D/K370S: S364K/E357L, K370S: S364K/E357Q, T366S/L368A/Y407V: T366W and T366S/L368A/Y407V/Y349C: T366W/S354C), optionally ablation variants (including those shown in FIG. 5), optionally charged scFv linkers (including those shown in FIGS. 7A-7B) and the heavy chain comprises pI variants (including those shown in FIG. 4).

In some embodiments, the bottle opener format includes skew variants, pI variants, and ablation variants. Accordingly, some embodiments include bottle opener formats that comprise: a) a first monomer (the “scFv monomer”) that comprises a charged scFv linker (with the +H sequence of FIGS. 7A-7B being preferred in some embodiments), the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, and an Fv that binds to PD-1 as outlined herein; b) a second monomer (the “Fab monomer”) that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, and a variable heavy domain that, with the variable light domain, makes up an Fv that binds to a second antigen as outlined herein; and c) a light chain.

A number of suitable combinations are outlined in WO2017/218707 for this format. Generally, the present invention is directed to the use of new anti-PD-1 ABDs based on a newly identified clone, 1C11. In this case, the heterodimeric antibodies bind to PD-1 and a second target antigen selected from the group consisting of CTLA-4, LAG-3, TIM-3, BTLA, TIGIT (all of which are classified as checkpoint receptors) and ICOS (which is an activator).

In some embodiments, the anti-PD-1 ABD is the scFv side of the bottle opener format. Thus, suitable ABD pairs include (scFv first, Fab second), PD-1×CTLA-4, PD-1×LAG-3, PD-1×TIM-3, PD-1×BTLA, PD-1×TIGIT and PD-1×ICOS. Suitable CDR sets as well as ABDs are described below, with particularly useful combinations similarly described below.

In some embodiments, the bottle opener format includes skew variants, pI variants, ablation variants and FcRn variants. Accordingly, some embodiments include bottle opener formats that comprise: a) a first monomer (the “scFv monomer”) that comprises a charged scFv linker (with the +H sequence of FIGS. 7A-7B being preferred in some embodiments), the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and an Fv that binds to PD-1 as outlined herein; b) a second monomer (the “Fab monomer”) that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a variable heavy domain that, with the variable light domain, makes up an Fv that binds to an antigen as outlined herein; and c) a light chain.

Specifically, FIGS. 50A-50E shows some bottle opener “skeleton” sequences that have a PD-1 scFv monomer but are missing the Fab sequences that can be used on the other side. That is, Fv sequences for the Fab portion of any ABD for CTLA-4, TIM-3, LAG-3, BTLA-, TIGIT and ICOS as discussed herein.

Specific bottle opener embodiments are outlined below.

B. mAb-Fv

One heterodimeric scaffold that finds particular use in the present invention is the mAb-Fv format shown in FIG. 1. In this embodiment, the format relies on the use of a C-terminal attachment of an “extra” variable heavy domain to one monomer and the C-terminal attachment of an “extra” variable light domain to the other monomer, thus forming a third antigen binding domain, wherein the Fab portions of the two monomers bind a target antigen as outlined herein and the “extra” scFv domain binds PD-1.

In this embodiment, the first monomer comprises a first heavy chain, comprising a first variable heavy domain and a first constant heavy domain comprising a first Fc domain, with a first variable light domain covalently attached to the C-terminus of the first Fc domain using a domain linker (vh1-CH1-hinge-CH2-CH3-[optional linker]-vl2). The second monomer comprises a second variable heavy domain of the second constant heavy domain comprising a second Fc domain, and a third variable heavy domain covalently attached to the C-terminus of the second Fc domain using a domain linker (vj1-CH1-hinge-CH2-CH3-[optional linker]-vh2. The two C-terminally attached variable domains make up a Fv that binds PD-1. This embodiment further utilizes a common light chain comprising a variable light domain and a constant light domain that associates with the heavy chains to form two identical Fabs that bind a target antigen. As for many of the embodiments herein, these constructs include skew variants, pI variants, ablation variants, additional Fc variants, etc. as desired and described herein.

In addition, the Fc domains of the mAb-Fv format comprise skew variants (e.g. a set of amino acid substitutions as shown in FIGS. 3 and 8, with particularly useful skew variants being selected from the group consisting of S364K/E357Q: L368D/K370S; L368D/K370S: S364K; L368E/K370S: S364K; T411T/E360E/Q362E: D401K; L368D/K370S: S364K/E357L, K370S: S364K/E357Q, T366S/L368A/Y407V: T366W and T366S/L368A/Y407V/Y349C: T366W/S354C), optionally ablation variants (including those shown in FIG. 5), optionally charged scFv linkers (including those shown in FIG. 7) and the heavy chain comprises pI variants (including those shown in FIG. 4).

In some embodiments, the mAb-Fv format includes skew variants, pI variants, and ablation variants. Accordingly, some embodiments include mAb-Fv formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, and a first variable heavy domain that, with the first variable light domain of the light chain, makes up an Fv, and a second variable heavy domain; b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, and a first variable heavy domain that, with the first variable light domain, makes up the Fv, and a second variable light chain, that together with the second variable heavy domain forms an Fv (ABD) that binds to PD-1; and c) a light chain comprising a first variable light domain and a constant light domain.

In some embodiments, the mAb-Fv format includes skew variants, pI variants, ablation variants and FcRn variants. Accordingly, some embodiments include mAb-Fv formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a first variable heavy domain that, with the first variable light domain of the light chain, makes up an Fv that binds to an antigen, and a second variable heavy domain; b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a first variable heavy domain that, with the first variable light domain, makes up the Fv that binds to the antigen as outlined herein, and a second variable light chain, that together with the second variable heavy domain of the first monomer forms an Fv (ABD) that binds PD-1; and c) a light chain comprising a first variable light domain and a constant light domain.

C. mAb-scFv

One heterodimeric scaffold that finds particular use in the present invention is the mAb-scFv format shown in FIG. 1. In this embodiment, the format relies on the use of a C-terminal attachment of a scFv to one of the monomers, thus forming a third antigen binding domain, wherein the Fab portions of the two monomers bind one of the antigens outlined herein and the “extra” scFv domain binds PD-1. Thus, the first monomer comprises a first heavy chain (comprising a variable heavy domain and a constant domain), with a C-terminally covalently attached scFv comprising a scFv variable light domain, an scFv linker and a scFv variable heavy domain in either orientation (vh1-CH1-hinge-CH2-CH3-[optional linker]-vh2-scFv linker-vl2 or vh1-CH1-hinge-CH2-CH3-[optional linker]-vl2-scFv linker-vh2). This embodiment further utilizes a common light chain comprising a variable light domain and a constant light domain, that associates with the heavy chains to form two identical Fabs that bind the antigen. As for many of the embodiments herein, these constructs include skew variants, pI variants, ablation variants, additional Fc variants, etc. as desired and described herein.

In addition, the Fc domains of the mAb-scFv format comprise skew variants (e.g. a set of amino acid substitutions as shown in FIGS. 3 and 8, with particularly useful skew variants being selected from the group consisting of S364K/E357Q: L368D/K370S; L368D/K370S: S364K; L368E/K370S: S364K; T411T/E360E/Q362E: D401K; L368D/K370S: S364K/E357L, K370S: S364K/E357Q, T366S/L368A/Y407V: T366W and T366S/L368A/Y407V/Y349C: T366W/S354C), optionally ablation variants (including those shown in FIG. 5), optionally charged scFv linkers (including those shown in FIG. 7) and the heavy chain comprises pI variants (including those shown in FIG. 4).

In some embodiments, the mAb-scFv format includes skew variants, pI variants, and ablation variants. Accordingly, some embodiments include mAb-scFv formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, and a variable heavy domain that, with the variable light domain of the common light chain, makes up an Fv that binds to a target antigen as outlined herein, and a scFv domain that binds to PD-1; b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, and a variable heavy domain that, with the variable light domain of the common light chain, makes up an Fv that binds to the target antigen as outlined herein; and c) a common light chain comprising a variable light domain and a constant light domain.

In some embodiments, the mAb-scFv format includes skew variants, pI variants, ablation variants and FcRn variants. Accordingly, some embodiments include mAb-scFv formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a variable heavy domain that, with the variable light domain of the common light chain, makes up an Fv that binds to an antigen as outlined herein, and a scFv domain that binds to PD-1; b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a variable heavy domain that, with the variable light domain of the common light chain, makes up an Fv that binds to an antigen as outlined herein; and c) a common light chain comprising a variable light domain and a constant light domain.

D. Central-scFv

One heterodimeric scaffold that finds particular use in the present invention is the Central-scFv format shown in FIG. 1 (also sometimes referred to as the “2+1” format). In this embodiment, the format relies on the use of an inserted scFv domain thus forming a third antigen binding domain, wherein the Fab portions of the two monomers bind a target antigen and the “extra” scFv domain binds PD-1. The scFv domain is inserted between the Fc domain and the CH1-Fv region of one of the monomers, thus providing a third antigen binding domain. This can actually be thought of as an addition to the bottle opener format, wherein there is an additional VH-CH1 domain added to the N-terminus of the scFv, which utilizes a common light chain.

In this embodiment, one monomer comprises a first heavy chain comprising a first variable heavy domain, a CH1 domain (and optional hinge) and Fc domain, with a scFv comprising a scFv variable light domain, an scFv linker and a scFv variable heavy domain. The scFv is covalently attached between the C-terminus of the CH1 domain of the heavy constant domain and the N-terminus of the first Fc domain using optional domain linkers (vh1-CH1-[optional linker]-vh2-scFv linker-vl2-[optional linker including the hinge]-CH2-CH3, or the opposite orientation for the scFv, vh1-CH1-[optional linker]-vl2-scFv linker-vh2-[optional linker including the hinge]-CH2-CH3). The other monomer is a standard Fab side. This embodiment further utilizes a common light chain comprising a variable light domain and a constant light domain, that associates with the heavy chains to form two identical Fabs that bind a target antigen. As for many of the embodiments herein, these constructs include skew variants, pI variants, ablation variants, additional Fc variants, etc. as desired and described herein.

In addition, the Fc domains of the central scFv format comprise skew variants (e.g. a set of amino acid substitutions as shown in FIGS. 3 and 8, with particularly useful skew variants being selected from the group consisting of S364K/E357Q: L368D/K370S; L368D/K370S: S364K; L368E/K370S: S364K; T411T/E360E/Q362E: D401K; L368D/K370S: S364K/E357L, K370S: S364K/E357Q, T366S/L368A/Y407V: T366W and T366S/L368A/Y407V/Y349C: T366W/S354C), optionally ablation variants (including those shown in FIG. 5), optionally charged scFv linkers (including those shown in FIG. 7) and the heavy chain comprises pI variants (including those shown in FIG. 4).

In some embodiments, the central-scFv format includes skew variants, pI variants, and ablation variants. Accordingly, some embodiments include central scFv formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, and a variable heavy domain that, with the variable light domain of the light chain, makes up an Fv that binds to a target antigen as outlined herein, and an scFv domain that binds to PD-1; b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, and a variable heavy domain that, with variable light domain of the light chain, makes up an Fv that binds to a target antigen as outlined herein; and c) a light chain comprising a variable light domain and a constant light domain.

In some embodiments, the central-scFv format includes skew variants, pI variants, ablation variants and FcRn variants. Accordingly, some embodiments include central scFv formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a variable heavy domain that, with the variable light domain of the light chain, makes up an Fv that binds to a target antigen as outlined herein, and an scFv domain that binds to PD-1; b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a variable heavy domain that, with variable light domain of the light chain, makes up an Fv that binds to SSTR2 as outlined herein; and c) a light chain comprising a variable light domain and a constant light domain.

E. Central-Fv

One heterodimeric scaffold that finds particular use in the present invention is the Central-Fv format shown in FIG. 1G. In this embodiment, the format relies on the use of an inserted Fv domain (i.e., the central Fv domain) thus forming a third antigen binding domain, wherein the Fab portions of the two monomers bind a target antigen and the “central Fv” domain binds PD-1. The scFv domain is inserted between the Fc domain and the CH1-Fv region of the monomers, thus providing a third antigen binding domain, wherein each monomer contains a component of the scFv (e.g. one monomer comprises a variable heavy domain and the other a variable light domain).

In this embodiment, one monomer comprises a first heavy chain comprising a first variable heavy domain, a CH1 domain, and Fc domain and an additional variable light domain. The light domain is covalently attached between the C-terminus of the CH1 domain of the heavy constant domain and the N-terminus of the first Fc domain using domain linkers (vh1-CH1-[optional linker]-vl2-hinge-CH2-CH3). The other monomer comprises a first heavy chain comprising a first variable heavy domain, a CH1 domain and Fc domain and an additional variable heavy domain (vh1-CH1-[optional linker]-vh2-hinge-CH2-CH3). The light domain is covalently attached between the C-terminus of the CH1 domain of the heavy constant domain and the N-terminus of the first Fc domain using domain linkers.

This embodiment further utilizes a common light chain comprising a variable light domain and a constant light domain, that associates with the heavy chains to form two identical Fabs that bind a target antigen. As for many of the embodiments herein, these constructs include skew variants, pI variants, ablation variants, additional Fc variants, etc. as desired and described herein.

F. One Armed Central-scFv

One heterodimeric scaffold that finds particular use in the present invention is the one armed central-scFv format shown in FIG. 1. In this embodiment, one monomer comprises just an Fc domain, while the other monomer uses an inserted scFv domain thus forming the second antigen binding domain. In this format, either the Fab portion binds a target antigen and the scFv binds PD-1 or vice versa. The scFv domain is inserted between the Fc domain and the CH1-Fv region of one of the monomers.

In this embodiment, one monomer comprises a first heavy chain comprising a first variable heavy domain, a CH1 domain and Fc domain, with a scFv comprising a scFv variable light domain, an scFv linker and a scFv variable heavy domain. The scFv is covalently attached between the C-terminus of the CH1 domain of the heavy constant domain and the N-terminus of the first Fc domain using domain linkers. The second monomer comprises an Fc domain. This embodiment further utilizes a light chain comprising a variable light domain and a constant light domain, that associates with the heavy chain to form a Fab. As for many of the embodiments herein, these constructs include skew variants, pI variants, ablation variants, additional Fc variants, etc. as desired and described herein.

In addition, the Fc domains of the one armed central-scFv format generally include skew variants (e.g. a set of amino acid substitutions as shown in FIGS. 3 and 8, with particularly useful skew variants being selected from the group consisting of S364K/E357Q: L368D/K370S; L368D/K370S: S364K; L368E/K370S: S364K; T411T/E360E/Q362E: D401K; L368D/K370S: S364K/E357L, K370S: S364K/E357Q, T366S/L368A/Y407V: T366W and T366S/L368A/Y407V/Y349C: T366W/S354C), optionally ablation variants (including those shown in FIG. 5), optionally charged scFv linkers (including those shown in FIG. 7) and the heavy chain comprises pI variants (including those shown in FIG. 4).

In some embodiments, the one armed central-scFv format includes skew variants, pI variants, and ablation variants. Accordingly, some embodiments of the one armed central-scFv formats comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, and a variable heavy domain that, with the variable light domain of the light chain, makes up an Fv that binds to a target antigen as outlined herein, and a scFv domain that binds to PD-1; b) a second monomer that includes an Fc domain having the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K; and c) a light chain comprising a variable light domain and a constant light domain.

In some embodiments, the one armed central-scFv format includes skew variants, pI variants, ablation variants and FcRn variants. Accordingly, some embodiments of the one armed central-scFv formats comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a variable heavy domain that, with the variable light domain of the light chain, makes up an Fv that binds to a target antigen as outlined herein, and a scFv domain that binds to PD-1; b) a second monomer that includes an Fc domain having the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, and the FcRn variants M428L/N434S; and c) a light chain comprising a variable light domain and a constant light domain.

G. One Armed scFv-mAb

One heterodimeric scaffold that finds particular use in the present invention is the one armed scFv-mAb format shown in FIG. 1. In this embodiment, one monomer comprises just an Fc domain, while the other monomer uses a scFv domain attached at the N-terminus of the heavy chain, generally through the use of a linker: vh-scFv linker-vl-[optional domain linker]-CH1-hinge-CH2-CH3 or (in the opposite orientation) vl-scFv linker-vh-[optional domain linker]-CH1-hinge-CH2-CH3. In this format, the Fab portions each bind a target antigen and the scFv binds PD-1. This embodiment further utilizes a light chain comprising a variable light domain and a constant light domain, that associates with the heavy chain to form a Fab. As for many of the embodiments herein, these constructs include skew variants, pI variants, ablation variants, additional Fc variants, etc. as desired and described herein.

In addition, the Fc domains of the one armed scFv-mAb format generally include skew variants (e.g. a set of amino acid substitutions as shown in FIGS. 3 and 8, with particularly useful skew variants being selected from the group consisting of S364K/E357Q: L368D/K370S; L368D/K370S: S364K; L368E/K370S: S364K; T411T/E360E/Q362E: D401K; L368D/K370S: S364K/E357L, K370S: S364K/E357Q, T366S/L368A/Y407V: T366W and T366S/L368A/Y407V/Y349C: T366W/S354C), optionally ablation variants (including those shown in FIG. 5), optionally charged scFv linkers (including those shown in FIG. 7) and the heavy chain comprises pI variants (including those shown in FIG. 4).

In some embodiments, the one armed scFv-mAb format includes skew variants, pI variants, and ablation variants. Accordingly, some embodiments of the one armed scFv-mAb formats comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, and a variable heavy domain that, with the variable light domain of the light chain, makes up an Fv that binds to a target antigen as outlined herein, and a scFv domain that binds to PD-1; b) a second monomer that includes an Fc domain having the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K; and c) a light chain comprising a variable light domain and a constant light domain.

In some embodiments, the one armed scFv-mAb format includes skew variants, pI variants, ablation variants and FcRn variants. Accordingly, some embodiments one armed scFv-mAb formats comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a variable heavy domain that, with the variable light domain of the light chain, makes up an Fv that binds to a target antigen as outlined herein, and a scFv domain that binds to PD-1; b) a second monomer that includes an Fc domain having the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, and the FcRn variants M428L/N434S; and c) a light chain comprising a variable light domain and a constant light domain.

H. scFv-mAb

One heterodimeric scaffold that finds particular use in the present invention is the mAb-scFv format shown in FIG. 1E. In this embodiment, the format relies on the use of a N-terminal attachment of a scFv to one of the monomers, thus forming a third antigen binding domain, wherein the Fab portions of the two monomers bind a target antigen and the “extra” scFv domain binds PD-1.

In this embodiment, the first monomer comprises a first heavy chain (comprising a variable heavy domain and a constant domain), with a N-terminally covalently attached scFv comprising a scFv variable light domain, an scFv linker and a scFv variable heavy domain in either orientation ((vh1-scFv linker-vl1-[optional domain linker]-vh2-CH1-hinge-CH2-CH3) or (with the scFv in the opposite orientation) ((vl1-scFv linker-vh1-[optional domain linker]-vh2-CH1-hinge-CH2-CH3)). This embodiment further utilizes a common light chain comprising a variable light domain and a constant light domain that associates with the heavy chains to form two identical Fabs that bind the target. As for many of the embodiments herein, these constructs include skew variants, pI variants, ablation variants, additional Fc variants, etc. as desired and described herein.

In addition, the Fc domains of the scFv-mAb format generally include skew variants (e.g. a set of amino acid substitutions as shown in FIGS. 3 and 8, with particularly useful skew variants being selected from the group consisting of S364K/E357Q: L368D/K370S; L368D/K370S: S364K; L368E/K370S: S364K; T411T/E360E/Q362E: D401K; L368D/K370S: S364K/E357L, K370S: S364K/E357Q, T366S/L368A/Y407V: T366W and T366S/L368A/Y407V/Y349C: T366W/S354C), optionally ablation variants (including those shown in FIG. 5), optionally charged scFv linkers (including those shown in FIG. 7) and the heavy chain comprises pI variants (including those shown in FIG. 4).

In some embodiments, the scFv-mAb format includes skew variants, pI variants, and ablation variants. Accordingly, some embodiments include scFv-mAb formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, and a variable heavy domain that, with the variable light domain of the common light chain, makes up an Fv that binds to the target as outlined herein, and a scFv domain that binds to PD-1; b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, and a variable heavy domain that, with the variable light domain of the common light chain, makes up an Fv that binds to the target antigen as outlined herein; and c) a common light chain comprising a variable light domain and a constant light domain.

In some embodiments, the scFv-mAb format includes skew variants, pI variants, ablation variants and FcRn variants. Accordingly, some embodiments include scFv-mAb formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a variable heavy domain that, with the variable light domain of the common light chain, makes up an Fv that binds to the target antigen as outlined herein, and a scFv domain that binds to PD-1; b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a variable heavy domain that, with the variable light domain of the common light chain, makes up an Fv that binds to the target as outlined herein; and c) a common light chain comprising a variable light domain and a constant light domain.

I. Dual scFv Formats

The present invention also provides dual scFv formats as are known in the art and shown in FIG. 1B. In this embodiment, the SSTR2×CD3 heterodimeric bispecific antibody is made up of two scFv-Fc monomers (both in either (vh-scFv linker-vl-[optional domain linker]-CH2-CH3) format or (vl-scFv linker-vh-[optional domain linker]-CH2-CH3) format, or with one monomer in one orientation and the other in the other orientation.

In some embodiments, the dual scFv format includes skew variants, pI variants, and ablation variants. Accordingly, some embodiments include dual scFv formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, and a first scFv that binds either PD-1 or the target antigen; and b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, and a second scFv that binds either PD-1 or the other target antigen.

In some embodiments, the dual scFv format includes skew variants, pI variants, ablation variants and FcRn variants. In some embodiments, the dual scFv format includes skew variants, pI variants, and ablation variants. Accordingly, some embodiments include dual scFv formats that comprise: a) a first monomer that comprises the skew variants S364K/E357Q, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a first scFv; and b) a second monomer that comprises the skew variants L368D/K370S, the pI variants N208D/Q295E/N384D/Q418E/N421D, the ablation variants E233P/L234V/L235A/G236del/S267K, the FcRn variants M428L/N434S and a second scFv.

XI. PARTICULAR EMBODIMENTS OF THE INVENTION

As will be appreciated by those in the art, the invention provides a large number of possible combinations of anti-PD-1 scFv sequences with the ABDs for different target antigens in the different formats of the invention.

In some embodiments, any PD-1 ABD of FIGS. 13, 15, 16, 18, 20, 21, 24, 33 and 40 can be combined with any anti-TIM-3 ABD, any anti-CTLA-4 ABD, any anti-ICOS ABD, any anti-TIM-3 ABD, any anti-LAG-3 ABD or any anti-BTLA ABD, in any format of FIG. 1. Of particular use are anti-PD-1 scFv sequences of FIG. 15 in combination with Fab ABDs of the sequence listing for these ABDs. In some embodiments, these combinations are made using the “backbone” sequences for the bottle opener format as depicted in FIG. 162 of US Publication No. 2016/0355608 (which can also be used for the Central-scFv format), or using the “backbone” sequences for the “mAb-scFv” format as depicted in FIG. 163 of US Publication No. 2016/0355608, both Figures of which (and the accompanying legends) are expressly incorporated by reference herein.

A. PD-1×CTLA-4 Bottle Opener Embodiments

In some embodiments, the invention provides bispecific heterodimeric antibodies that bind to both human PD-1 and human CTLA-4. As will be appreciated by those in the art, there are a large number of possible combinations of anti-PD-1 scFv sequences with the ABDs for CTLA-4.

In some embodiments, the PD-1 ABD is the scFv and the CTLA-4 ABD is the Fab construct. In these embodiments, any scFv ABD from FIG. 15 A-15T can be combined with any anti-CTLA-4 ABD sequence. Anti-CTLA-4 ABDs sequences suitable for use in the present invention include SEQ ID NOs: 21-2918 (CTLA-4 scFv sequences, although the Fv sequences therein can be formatted as Fabs), SEQ ID NOs: 2919-6208 (CTLA-4 Fab sequences, although the Fv sequences therein can be formatted as scFvs), SEQ ID NOs: 36739-36818 (additional CTLA-4 Fab sequences, although the Fv sequences therein can be formatted as scFvs) and SEQ ID NOs: 35395-35416 (CTLA-4 one armed constructs, which can be formatted as either Fabs or scFvs). As will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers.

In some embodiments, heterodimeric antibodies of the invention are made in the bottle opener format using a PD-1 ABD from FIG. 15 as the scFv and the CTLA-4 ABD as the Fab Fv, when the CTLA-4 ABD is selected from a pair from SEQ ID NOs:2919-6208 and SEQ ID NOs:35395-35416 of the present sequencing listing. In some embodiments, the VH domain of the CTLA-4 Fab is added to SEQ ID NO:471, the VL of the CTLA-4 Fab is added to SEQ ID NO:473 and the PD-1 scFv is added to SEQ ID NO:472 of US2016/0355608. In some embodiments, the VH domain of the CTLA-4 Fab is added to SEQ ID NO:474, the VL of the CTLA-4 Fab is added to SEQ ID NO:476 and the PD-1 scFv is added to SEQ ID NO:475 of US2016/0355608. In some embodiments, the VH domain of the CTLA-4 Fab is added to SEQ ID NO:477, the VL of the CTLA-4 Fab is added to SEQ ID NO:479 and the PD-1 scFv is added to SEQ ID NO:478 of US2016/0355608. In some embodiments, the VH domain of the CTLA-4 Fab is added to SEQ ID NO:480, the VL of the CTLA-4 Fab is added to SEQ ID NO:482 and the PD-1 scFv is added to SEQ ID NO:481 of US2016/0355608.

In some embodiments, the CTLA-4 Fab comprises a variable heavy domain of SEQ ID NO:38134 and a variable light domain of SEQ ID NO:38138.

In some embodiments, an anti-CTLA-4 Fab is selected from any of SEQ ID NOs: 2919-6208 and SEQ ID NOs: 36739-36818 herein, with the CTLA-4 Fab comprising a variable heavy domain of SEQ ID NO:38134 and a variable light domain of SEQ ID NO:38138 finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS556 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS556 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS556.

In some embodiments, an anti-CTLA-4 Fab is selected from any of SEQ ID NOs: 2919-6208 and SEQ ID NOs: 36739-36818 herein, with the CTLA-4 Fab comprising a variable heavy domain of SEQ ID NO:38134 and a variable light domain of SEQ ID NO:38138 finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS557 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS557 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS557.

In some embodiments, an anti-CTLA-4 Fab is selected from any of SEQ ID NOs: 2919-6208 and SEQ ID NOs: 36739-36818 herein, with the CTLA-4 Fab comprising a variable heavy domain of SEQ ID NO:38134 and a variable light domain of SEQ ID NO:38138 finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS558 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS558 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS558.

In some embodiments, an anti-CTLA-4 Fab is selected from any of SEQ ID NOs: 2919-6208 and SEQ ID NOs: 36739-36818 herein, with the CTLA-4 Fab comprising a variable heavy domain of SEQ ID NO:38134 and a variable light domain of SEQ ID NO:38138 finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS559 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS559 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS559.

In some embodiments, an anti-CTLA-4 Fab is selected from any of SEQ ID NOs: 2919-6208 and SEQ ID NOs: 36739-36818 herein, with the CTLA-4 Fab comprising a variable heavy domain of SEQ ID NO:38134 and a variable light domain of SEQ ID NO:38138 finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS560 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS560 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS560.

In some embodiments, an anti-CTLA-4 Fab is selected from any of SEQ ID NOs: 2919-6208 and SEQ ID NOs: 36739-36818 herein, with the CTLA-4 Fab comprising a variable heavy domain of SEQ ID NO:38134 and a variable light domain of SEQ ID NO:38138 finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS561 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS561 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS561.

In some embodiments, an anti-CTLA-4 Fab is selected from any of SEQ ID NOs: 2919-6208 and SEQ ID NOs: 36739-36818 herein, with the CTLA-4 Fab comprising a variable heavy domain of SEQ ID NO:38134 and a variable light domain of SEQ ID NO:38138 finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS562 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS562 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS562.

In some embodiments, an anti-CTLA-4 Fab is selected from any of SEQ ID NOs: 2919-6208 and SEQ ID NOs: 36739-36818 herein, with the CTLA-4 Fab comprising a variable heavy domain of SEQ ID NO:38134 and a variable light domain of SEQ ID NO:38138 finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS563 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS563 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS563.

In some embodiments, an anti-CTLA-4 Fab is selected from the pairs of SEQ ID NOs:36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807 and 36811 and 36815 of the sequence listing. In these embodiments, the remainder of the heterodimeric antibody is XENCS556 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS556 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS556.

In some embodiments, an anti-CTLA-4 Fab is selected from the pairs of SEQ ID NOs:36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807 and 36811 and 36815 of the sequence listing. In these embodiments, the remainder of the heterodimeric antibody is XENCS557 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS557 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS557.

In some embodiments, an anti-CTLA-4 Fab is selected from the pairs of SEQ ID NOs:36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807 and 36811 and 36815 of the sequence listing. In these embodiments, the remainder of the heterodimeric antibody is XENCS558 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS558 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS558.

In some embodiments, an anti-CTLA-4 Fab is selected from the pairs of SEQ ID NOs:36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807 and 36811 and 36815 of the sequence listing. In these embodiments, the remainder of the heterodimeric antibody is XENCS559 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS559 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS559.

In some embodiments, an anti-CTLA-4 Fab is selected from the pairs of SEQ ID NOs:36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807 and 36811 and 36815 of the sequence listing. In these embodiments, the remainder of the heterodimeric antibody is XENCS560 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS560 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS560.

In some embodiments, an anti-CTLA-4 Fab is selected from the pairs of SEQ ID NOs:36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807 and 36811 and 36815 of the sequence listing. In these embodiments, the remainder of the heterodimeric antibody is XENCS561 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS561 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS561.

In some embodiments, an anti-CTLA-4 Fab is selected from the pairs of SEQ ID NOs:36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807 and 36811 and 36815 of the sequence listing. In these embodiments, the remainder of the heterodimeric antibody is XENCS562 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS562 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS562.

In some embodiments, an anti-CTLA-4 Fab is selected from the pairs of SEQ ID NOs:36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807 and 36811 and 36815 of the sequence listing. In these embodiments, the remainder of the heterodimeric antibody is XENCS563 from FIG. 50; that is, the VH from the CTLA-4 Fab is added N-terminally to the Fab Chain of XENCS563 and the VL from the CTLA-4 Fab is added N-terminally to the Light Chain of XENCS563.

In some embodiments, the PD-1×CTLA-4 heterodimeric antibody of the invention is selected from the group consisting of XENCS502, XENCS509, XENCS516, XENCS523, XENCS530, XENCS537, XENCS544 and XENCS551.

B. PD-1×ICOS Bottle Opener Embodiments

In some embodiments, the invention provides bispecific heterodimeric antibodies that bind to both human PD-1 and human ICOS. As will be appreciated by those in the art, there are a large number of possible combinations of anti-PD-1 scFv sequences with the ABDs for ICOS.

In some embodiments, the PD-1 ABD is the scFv and the ICOS ABD is the Fab construct. In these embodiments, any scFv ABD from FIG. 15A-15T can be combined with any anti-ICOS ABD sequence. Anti-ICOS sequences suitable for use as ABDs include many as disclosed in US2018/0127501, expressly incorporated by reference in its entirety and specifically for the legends and FIGS. 19, 20 and 24, the sequences depicted therein, as well as SEQ ID NOs:27869-28086 from US2018/0127501 which contain a number of ICOS Fab sequences (heavy chain VH1-CH1 and light chain VL1-CL) as indicated in the naming nomenclature. Additionally included are the anti-ICOS ABDs of the VH/VL pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501. As will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers.

Of particular interest in the present invention are the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK, with VH_ICOS_H0_L0 and VL_ICOS_H0_L0. Of particular interest in the present invention are the Fab sequences of the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK, with VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0.

In some embodiments, the VH domain of the ICOS Fab is added to SEQ ID NO:471, the VL of the ICOS Fab is added to SEQ ID NO:473 and the PD-1 scFv is added to SEQ ID NO:472 of US2016/0355608. In some embodiments, the VH domain of the ICOS Fab is added to SEQ ID NO:474, the VL of the ICOS Fab is added to SEQ ID NO:476 and the PD-1 scFv is added to SEQ ID NO:475 of US2016/0355608. In some embodiments, the VH domain of the ICOS Fab is added to SEQ ID NO:477, the VL of the ICOS Fab is added to SEQ ID NO:479 and the PD-1 scFv is added to SEQ ID NO:478 of US2016/0355608. In some embodiments, the VH domain of the ICOS Fab is added to SEQ ID NO:480, the VL of the ICOS Fab is added to SEQ ID NO:482 and the PD-1 scFv is added to SEQ ID NO:481 of US2016/0355608.

In some embodiments, an anti-ICOS Fab is selected from VH/VL pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501, with the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK (VH_ICOS_H0_L0 and VL_ICOS_H0_L0) and the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK (VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS556 from FIG. 50; that is, the VH from the ICOS Fab is added N-terminally to the Fab Chain of XENCS556 and the VL from the ICOS Fab is added N-terminally to the Light Chain of XENCS556.

In some embodiments, an anti-ICOS Fab is selected from VH/VL pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501, with the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK (VH_ICOS_H0_L0 and VL_ICOS_H0_L0) and the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK (VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS557 from FIG. 50; that is, the VH from the ICOS Fab is added N-terminally to the Fab Chain of XENCS557 and the VL from the ICOS Fab is added N-terminally to the Light Chain of XENCS557.

In some embodiments, an anti-ICOS Fab is selected from VH/VL pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501, with the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK (VH_ICOS_H0_L0 and VL_ICOS_H0_L0) and the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK (VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS558 from FIG. 50; that is, the VH from the ICOS Fab is added N-terminally to the Fab Chain of XENCS558 and the VL from the ICOS Fab is added N-terminally to the Light Chain of XENCS558.

In some embodiments, an anti-ICOS Fab is selected from VH/VL pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501, with the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK (VH_ICOS_H0_L0 and VL_ICOS_H0_L0) and the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK (VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS559 from FIG. 50; that is, the VH from the ICOS Fab is added N-terminally to the Fab Chain of XENCS559 and the VL from the ICOS Fab is added N-terminally to the Light Chain of XENCS559.

In some embodiments, an anti-ICOS Fab is selected from VH/VL pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501, with the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK (VH_ICOS_H0_L0 and VL_ICOS_H0_L0) and the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK (VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS560 from FIG. 50; that is, the VH from the ICOS Fab is added N-terminally to the Fab Chain of XENCS560 and the VL from the ICOS Fab is added N-terminally to the Light Chain of XENCS560.

In some embodiments, an anti-ICOS Fab is selected from VH/VL pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501, with the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK (VH_ICOS_H0_L0 and VL_ICOS_H0_L0) and the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK (VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS561 from FIG. 50; that is, the VH from the ICOS Fab is added N-terminally to the Fab Chain of XENCS561 and the VL from the ICOS Fab is added N-terminally to the Light Chain of XENCS561.

In some embodiments, an anti-ICOS Fab is selected from VH/VL pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501, with the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK (VH_ICOS_H0_L0 and VL_ICOS_H0_L0) and the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK (VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS562 from FIG. 50; that is, the VH from the ICOS Fab is added N-terminally to the Fab Chain of XENCS562 and the VL from the ICOS Fab is added N-terminally to the Light Chain of XENCS562.

In some embodiments, an anti-ICOS Fab is selected from VH/VL pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501, with the Fab sequences of the anti-ICOS ABD from XENCS500 in FIGS. 49A-49KK (VH_ICOS_H0_L0 and VL_ICOS_H0_L0) and the anti-ICOS ABD from XENCS501 in FIGS. 49A-49KK (VH_ICOS_H0.66_L0 and VL_ICOS_H0.66_L0) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS563 from FIG. 50; that is, the VH from the ICOS Fab is added N-terminally to the Fab Chain of XENCS563 and the VL from the ICOS Fab is added N-terminally to the Light Chain of XENCS563.

In some embodiments, the PD-1×ICOS heterodimeric antibody of the invention is selected from the group consisting of XENCS500, XENCS501, XENCS507, XENCS508, XENCS514, XENCS515, XENCS521, XENCS522, XENCS528, XENCS529, XENCS535, XENCS526, XENCS542, XENCS543, XENCS549 and XENCS550.

C. PD-1×LAG-3 Bottle Opener Embodiments

In some embodiments, the invention provides bispecific heterodimeric antibodies that bind to both human PD-1 and human LAG-3. As will be appreciated by those in the art, there are a large number of possible combinations of anti-PD-1 scFv sequences with the ABDs for LAG-3.

In some embodiments, the PD-1 ABD is the scFv and the LAG-3 ABD is the Fab construct. In these embodiments, any scFv ABD from FIG. 15A-15T can be combined with any anti-LAG-3 ABD sequence. Anti-LAG-3 sequences suitable for use as ABDs include SEQ ID NOs: 17135-20764; SEQ ID NOs: 36819-36962; SEQ ID NOs: 35417-35606; SEQ ID NOs: 25194-32793; SEQ ID NOs: 32794-33002 (as will be understood from those in the art, all of these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-LAG-3 Fabs selected the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; as well as the sequences of the LAG-3 Fab ABD of XENP22594, including the VH (SEQ ID NO:32755, with VHCDRs (SEQ ID NOs:32756, 32757 and 32758) and VL (SEQ ID NO:32760 with VLCDRs (SEQ ID NOs:32761, 32762 and 32763) and the sequences of the LAG-3 Fab ABD of XENP22656, including the VH (SEQ ID NO:28815, with VHCDRs (SEQ ID NOs:28816, 28817, and 28118) and VL (SEQ ID NO:28820, with VLCDRs (SEQ ID NOs:28821, 28822 and 28823).

In some embodiments, the VH domain of the LAG-3 Fab is added to SEQ ID NO:471, the VL of the LAG-3 Fab is added to SEQ ID NO:473 and the PD-1 scFv is added to SEQ ID NO:472 of US2016/0355608. In some embodiments, the VH domain of the LAG-3 Fab is added to SEQ ID NO:474, the VL of the LAG-3 Fab is added to SEQ ID NO:476 and the PD-1 scFv is added to SEQ ID NO:475 of US2016/0355608. In some embodiments, the VH domain of the LAG-3 Fab is added to SEQ ID NO:477, the VL of the LAG-3 Fab is added to SEQ ID NO:479 and the PD-1 scFv is added to SEQ ID NO:478 of US2016/0355608. In some embodiments, the VH domain of the LAG-3 Fab is added to SEQ ID NO:480, the VL of the LAG-3 Fab is added to SEQ ID NO:482 and the PD-1 scFv is added to SEQ ID NO:481 of US2016/0355608.

In some embodiments, the anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; with the VH/VL of XENP22594 (VH SEQ ID NO:32755 and VL SEQ ID NO:32760) and the VH/VL of XENP22656 (VH SEQ ID NO:28815 VL SEQ ID NO:28820) finding particular use.

In some embodiments, the anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; with the VH/VL of XENP22594 (VH SEQ ID NO:32755 and VL SEQ ID NO:32760) and the VH/VL of XENP22656 (VH SEQ ID NO:28815 VL SEQ ID NO:28820) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS556 from FIG. 50; that is, the VH from the LAG-3 Fab is added N-terminally to the Fab Chain of XENCS556 and the VL from the LAG-3 Fab is added N-terminally to the Light Chain of XENCS556.

In some embodiments, the anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; with the VH/VL of XENP22594 (VH SEQ ID NO:32755 and VL SEQ ID NO:32760) and the VH/VL of XENP22656 (VH SEQ ID NO:28815 VL SEQ ID NO:28820) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS557 from FIG. 50; that is, the VH from the LAG-3 Fab is added N-terminally to the Fab Chain of XENCS557 and the VL from the LAG-3 Fab is added N-terminally to the Light Chain of XENCS557.

In some embodiments, the anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; with the VH/VL of XENP22594 (VH SEQ ID NO:32755 and VL SEQ ID NO:32760) and the VH/VL of XENP22656 (VH SEQ ID NO:28815 VL SEQ ID NO:28820) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS558 from FIG. 50; that is, the VH from the LAG-3 Fab is added N-terminally to the Fab Chain of XENCS558 and the VL from the LAG-3 Fab is added N-terminally to the Light Chain of XENCS558.

In some embodiments, the anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; with the VH/VL of XENP22594 (VH SEQ ID NO:32755 and VL SEQ ID NO:32760) and the VH/VL of XENP22656 (VH SEQ ID NO:28815 VL SEQ ID NO:28820) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS559 from FIG. 50; that is, the VH from the LAG-3 Fab is added N-terminally to the Fab Chain of XENCS559 and the VL from the LAG-3 Fab is added N-terminally to the Light Chain of XENCS559.

In some embodiments, the anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; with the VH/VL of XENP22594 (VH SEQ ID NO:32755 and VL SEQ ID NO:32760) and the VH/VL of XENP22656 (VH SEQ ID NO:28815 VL SEQ ID NO:28820) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS560 from FIG. 50; that is, the VH from the LAG-3 Fab is added N-terminally to the Fab Chain of XENCS560 and the VL from the LAG-3 Fab is added N-terminally to the Light Chain of XENCS560.

In some embodiments, the anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; with the VH/VL of XENP22594 (VH SEQ ID NO:32755 and VL SEQ ID NO:32760) and the VH/VL of XENP22656 (VH SEQ ID NO:28815 VL SEQ ID NO:28820) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS561 from FIG. 50; that is, the VH from the LAG-3 Fab is added N-terminally to the Fab Chain of XENCS561 and the VL from the LAG-3 Fab is added N-terminally to the Light Chain of XENCS561.

In some embodiments, the anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; with the VH/VL of XENP22594 (VH SEQ ID NO:32755 and VL SEQ ID NO:32760) and the VH/VL of XENP22656 (VH SEQ ID NO:28815 VL SEQ ID NO:28820) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS562 from FIG. 50; that is, the VH from the LAG-3 Fab is added N-terminally to the Fab Chain of XENCS562 and the VL from the LAG-3 Fab is added N-terminally to the Light Chain of XENCS562.

In some embodiments, the anti-LAG-3 Fab is selected from the pairs of SEQ ID NOs:36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and 36959; with the VH/VL of XENP22594 (VH SEQ ID NO:32755 and VL SEQ ID NO:32760) and the VH/VL of XENP22656 (VH SEQ ID NO:28815 VL SEQ ID NO:28820) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS563 from FIG. 50; that is, the VH from the LAG-3 Fab is added N-terminally to the Fab Chain of XENCS563 and the VL from the LAG-3 Fab is added N-terminally to the Light Chain of XENCS563.

In some embodiments, the PD-1×LAG-3 heterodimeric antibody of the invention is selected from the group consisting of XENCS503, XENCS504, XENCS510, XENCS511, XENCS517, XENCS518, XENCS521, XENCS524, XENCS525, XENCS531, XENCS532, XENCS538, XENCS539, XENCS545, XENCS546, XENCS552 and XENCS553.

D. PD-1×TIM-3 Bottle Opener Embodiments

In some embodiments, the invention provides bispecific heterodimeric antibodies that bind to both human PD-1 and human TIM-3. As will be appreciated by those in the art, there are a large number of possible combinations of anti-PD-1 scFv sequences with the ABDs for TIM-3.

In some embodiments, the PD-1 ABD is the scFv and the TIM-3 ABD is the Fab construct. In these embodiments, any scFv ABD from FIG. 15A-15T can be combined with any anti-TIM-3 ABD sequence. Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884; SEQ ID NOs: 37587-37698; SEQ ID NOs: 36347-36706 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), anti-TIM-3 ABDs selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695; as well as the Fab sequences of the anti-TIM-3 ABD of XENP21189 (VH SEQ ID NO:36508 and VL SEQ ID NO:36513) finding particular use.

In some embodiments, the VH domain of the TIM-3 Fab is added to SEQ ID NO:471, the VL of the TIM-3 Fab is added to SEQ ID NO:473 and the PD-1 scFv is added to SEQ ID NO:472 of US2016/0355608. In some embodiments, the VH domain of the TIM-3 Fab is added to SEQ ID NO:474, the VL of the TIM-3 Fab is added to SEQ ID NO:476 and the PD-1 scFv is added to SEQ ID NO:475 of US2016/0355608. In some embodiments, the VH domain of the TIM-3 Fab is added to SEQ ID NO:477, the VL of the TIM-3 Fab is added to SEQ ID NO:479 and the PD-1 scFv is added to SEQ ID NO:478 of US2016/0355608. In some embodiments, the VH domain of the TIM-3 Fab is added to SEQ ID NO:480, the VL of the TIM-3 Fab is added to SEQ ID NO:482 and the PD-1 scFv is added to SEQ ID NO:481 of US2016/0355608.

Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884; SEQ ID NOs: 37587-37698; SEQ ID NOs: 36347-36706 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), anti-TIM-3 ABDs selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695; as well as the Fab sequences of the anti-TIM-3 ABD of XENP21189 (VH SEQ ID NO:36508 and VL SEQ ID NO:36513) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS556 from FIG. 50; that is, the VH from the TIM-3 Fab is added N-terminally to the Fab Chain of XENCS556 and the VL from the TIM-3 Fab is added N-terminally to the Light Chain of XENCS556.

Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884; SEQ ID NOs: 37587-37698; SEQ ID NOs: 36347-36706 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), anti-TIM-3 ABDs selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695; as well as the Fab sequences of the anti-TIM-3 ABD of XENP21189 (VH SEQ ID NO:36508 and VL SEQ ID NO:36513) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS557 from FIG. 50; that is, the VH from the TIM-3 Fab is added N-terminally to the Fab Chain of XENCS557 and the VL from the TIM-3 Fab is added N-terminally to the Light Chain of XENCS557.

Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884; SEQ ID NOs: 37587-37698; SEQ ID NOs: 36347-36706 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), anti-TIM-3 ABDs selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695; as well as the Fab sequences of the anti-TIM-3 ABD of XENP21189 (VH SEQ ID NO:36508 and VL SEQ ID NO:36513) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS558 from FIG. 50; that is, the VH from the TIM-3 Fab is added N-terminally to the Fab Chain of XENCS558 and the VL from the TIM-3 Fab is added N-terminally to the Light Chain of XENCS558.

Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884; SEQ ID NOs: 37587-37698; SEQ ID NOs: 36347-36706 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), anti-TIM-3 ABDs selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695; as well as the Fab sequences of the anti-TIM-3 ABD of XENP21189 (VH SEQ ID NO:36508 and VL SEQ ID NO:36513) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS559 from FIG. 50; that is, the VH from the TIM-3 Fab is added N-terminally to the Fab Chain of XENCS559 and the VL from the TIM-3 Fab is added N-terminally to the Light Chain of XENCS559.

Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884; SEQ ID NOs: 37587-37698; SEQ ID NOs: 36347-36706 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), anti-TIM-3 ABDs selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695; as well as the Fab sequences of the anti-TIM-3 ABD of XENP21189 (VH SEQ ID NO:36508 and VL SEQ ID NO:36513) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS560 from FIG. 50; that is, the VH from the TIM-3 Fab is added N-terminally to the Fab Chain of XENCS560 and the VL from the TIM-3 Fab is added N-terminally to the Light Chain of XENCS560.

Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884; SEQ ID NOs: 37587-37698; SEQ ID NOs: 36347-36706 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), anti-TIM-3 ABDs selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695; as well as the Fab sequences of the anti-TIM-3 ABD of XENP21189 (VH SEQ ID NO:36508 and VL SEQ ID NO:36513) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS561 from FIG. 50; that is, the VH from the TIM-3 Fab is added N-terminally to the Fab Chain of XENCS561 and the VL from the TIM-3 Fab is added N-terminally to the Light Chain of XENCS561.

Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884; SEQ ID NOs: 37587-37698; SEQ ID NOs: 36347-36706 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), anti-TIM-3 ABDs selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695; as well as the Fab sequences of the anti-TIM-3 ABD of XENP21189 (VH SEQ ID NO:36508 and VL SEQ ID NO:36513) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS562 from FIG. 50; that is, the VH from the TIM-3 Fab is added N-terminally to the Fab Chain of XENCS562 and the VL from the TIM-3 Fab is added N-terminally to the Light Chain of XENCS562.

Anti-TIM-3 sequences suitable for use as ABDs include SEQ ID NOs: 20765-20884; SEQ ID NOs: 37587-37698; SEQ ID NOs: 36347-36706 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), anti-TIM-3 ABDs selected from the pairs of SEQ ID NOs:35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and 37695; as well as the Fab sequences of the anti-TIM-3 ABD of XENP21189 (VH SEQ ID NO:36508 and VL SEQ ID NO:36513) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS563 from FIG. 50; that is, the VH from the TIM-3 Fab is added N-terminally to the Fab Chain of XENCS563 and the VL from the TIM-3 Fab is added N-terminally to the Light Chain of XENCS563.

In some embodiments, the PD-1×TIM-3 heterodimeric antibody of the invention is selected from the group consisting of XENCS505, XENCS512, XENCS519, XENCS526, XENCS533, XENCS540, XENCS547 and XENCS554.

E. PD-1×TIGIT Bottle Opener Embodiments

In some embodiments, the invention provides bispecific heterodimeric antibodies that bind to both human PD-1 and human TIGIT. As will be appreciated by those in the art, there are a large number of possible combinations of anti-PD-1 scFv sequences with the ABDs for TIGIT.

In some embodiments, the PD-1 ABD is the scFv and the TIGIT ABD is the Fab construct. In these embodiments, any scFv ABD from FIG. 15A-15T can be combined with any anti-TIGIT ABD sequence. Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583.

In some embodiments, the VH domain of the TIGIT Fab is added to SEQ ID NO:471, the VL of the TIGIT Fab is added to SEQ ID NO:473 and the PD-1 scFv is added to SEQ ID NO:472 of US2016/0355608. In some embodiments, the VH domain of the TIGIT Fab is added to SEQ ID NO:474, the VL of the TIGIT Fab is added to SEQ ID NO:476 and the PD-1 scFv is added to SEQ ID NO:475 of US2016/0355608. In some embodiments, the VH domain of the TIGIT Fab is added to SEQ ID NO:477, the VL of the TIGIT Fab is added to SEQ ID NO:479 and the PD-1 scFv is added to SEQ ID NO:478 of US2016/0355608. In some embodiments, the VH domain of the TIGIT Fab is added to SEQ ID NO:480, the VL of the TIGIT Fab is added to SEQ ID NO:482 and the PD-1 scFv is added to SEQ ID NO:481 of US2016/0355608.

Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583. In these embodiments, the remainder of the heterodimeric antibody is XENCS556 from FIG. 50; that is, the VH from the TIGIT Fab is added N-terminally to the Fab Chain of XENCS556 and the VL from the TIGIT Fab is added N-terminally to the Light Chain of XENCS556.

Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583. In these embodiments, the remainder of the heterodimeric antibody is XENCS557 from FIG. 50; that is, the VH from the TIGIT Fab is added N-terminally to the Fab Chain of XENCS557 and the VL from the TIGIT Fab is added N-terminally to the Light Chain of XENCS557.

Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583. In these embodiments, the remainder of the heterodimeric antibody is XENCS558 from FIG. 50; that is, the VH from the TIGIT Fab is added N-terminally to the Fab Chain of XENCS558 and the VL from the TIGIT Fab is added N-terminally to the Light Chain of XENCS558.

Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583. In these embodiments, the remainder of the heterodimeric antibody is XENCS559 from FIG. 50; that is, the VH from the TIGIT Fab is added N-terminally to the Fab Chain of XENCS559 and the VL from the TIGIT Fab is added N-terminally to the Light Chain of XENCS559.

Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583. In these embodiments, the remainder of the heterodimeric antibody is XENCS560 from FIG. 50; that is, the VH from the TIGIT Fab is added N-terminally to the Fab Chain of XENCS560 and the VL from the TIGIT Fab is added N-terminally to the Light Chain of XENCS560.

Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583. In these embodiments, the remainder of the heterodimeric antibody is XENCS561 from FIG. 50; that is, the VH from the TIGIT Fab is added N-terminally to the Fab Chain of XENCS561 and the VL from the TIGIT Fab is added N-terminally to the Light Chain of XENCS561.

Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583. In these embodiments, the remainder of the heterodimeric antibody is XENCS562 from FIG. 50; that is, the VH from the TIGIT Fab is added N-terminally to the Fab Chain of XENCS562 and the VL from the TIGIT Fab is added N-terminally to the Light Chain of XENCS562.

Anti-TIGIT sequences suitable for use as ABDs include SEQ ID NOs: 21504-21523 and SEQ ID NOs: 37435-37586 (as will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers), as well as TIGIT ABDs selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and 37583. In these embodiments, the remainder of the heterodimeric antibody is XENCS563 from FIG. 50; that is, the VH from the TIGIT Fab is added N-terminally to the Fab Chain of XENCS563 and the VL from the TIGIT Fab is added N-terminally to the Light Chain of XENCS563.

F. PD-1×BTLA Bottle Opener Embodiments

In some embodiments, the PD-1 ABD is the scFv and the BTLA ABD is the Fab construct. In these embodiments, any scFv ABD from FIG. 15A-15T can be combined with any anti-BTLA ABD sequence Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 and SEQ ID NOs: 36707-36738 (s will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-BTLA ABD selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735; with the Fab anti-BTLA ABD of XENP20269 (VH SEQ ID NO:20936 and VL SEQ ID NO:20941) finding particular use.

In some embodiments, the VH domain of the BTLA Fab is added to SEQ ID NO:471, the VL of the BTLA Fab is added to SEQ ID NO:473 and the PD-1 scFv is added to SEQ ID NO:472 of US2016/0355608. In some embodiments, the VH domain of the BTLA Fab is added to SEQ ID NO:474, the VL of the BTLA Fab is added to SEQ ID NO:476 and the PD-1 scFv is added to SEQ ID NO:475 of US2016/0355608. In some embodiments, the VH domain of the BTLA Fab is added to SEQ ID NO:477, the VL of the BTLA Fab is added to SEQ ID NO:479 and the PD-1 scFv is added to SEQ ID NO:478 of US2016/0355608. In some embodiments, the VH domain of the BTLA Fab is added to SEQ ID NO:480, the VL of the BTLA Fab is added to SEQ ID NO:482 and the PD-1 scFv is added to SEQ ID NO:481 of US2016/0355608.

Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 and SEQ ID NOs: 36707-36738 (s will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-BTLA ABD selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735; with the Fab anti-BTLA ABD of XENP20269 (VH SEQ ID NO:20936 and VL SEQ ID NO:20941) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS556 from FIG. 50; that is, the VH from the BTLA Fab is added N-terminally to the Fab Chain of XENCS556 and the VL from the BTLA Fab is added N-terminally to the Light Chain of XENCS556.

Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 and SEQ ID NOs: 36707-36738 (s will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-BTLA ABD selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735; with the Fab anti-BTLA ABD of XENP20269 (VH SEQ ID NO:20936 and VL SEQ ID NO:20941) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS557 from FIG. 50; that is, the VH from the BTLA Fab is added N-terminally to the Fab Chain of XENCS557 and the VL from the BTLA Fab is added N-terminally to the Light Chain of XENCS557.

Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 and SEQ ID NOs: 36707-36738 (s will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-BTLA ABD selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735; with the Fab anti-BTLA ABD of XENP20269 (VH SEQ ID NO:20936 and VL SEQ ID NO:20941) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS558 from FIG. 50; that is, the VH from the BTLA Fab is added N-terminally to the Fab Chain of XENCS558 and the VL from the BTLA Fab is added N-terminally to the Light Chain of XENCS558.

Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 and SEQ ID NOs: 36707-36738 (s will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-BTLA ABD selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735; with the Fab anti-BTLA ABD of XENP20269 (VH SEQ ID NO:20936 and VL SEQ ID NO:20941) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS559 from FIG. 50; that is, the VH from the BTLA Fab is added N-terminally to the Fab Chain of XENCS559 and the VL from the BTLA Fab is added N-terminally to the Light Chain of XENCS559.

Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 and SEQ ID NOs: 36707-36738 (s will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-BTLA ABD selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735; with the Fab anti-BTLA ABD of XENP20269 (VH SEQ ID NO:20936 and VL SEQ ID NO:20941) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS560 from FIG. 50; that is, the VH from the BTLA Fab is added N-terminally to the Fab Chain of XENCS560 and the VL from the BTLA Fab is added N-terminally to the Light Chain of XENCS560.

Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 and SEQ ID NOs: 36707-36738 (s will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-BTLA ABD selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735; with the Fab anti-BTLA ABD of XENP20269 (VH SEQ ID NO:20936 and VL SEQ ID NO:20941) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS561 from FIG. 50; that is, the VH from the BTLA Fab is added N-terminally to the Fab Chain of XENCS561 and the VL from the BTLA Fab is added N-terminally to the Light Chain of XENCS561.

Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 and SEQ ID NOs: 36707-36738 (s will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-BTLA ABD selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735; with the Fab anti-BTLA ABD of XENP20269 (VH SEQ ID NO:20936 and VL SEQ ID NO:20941) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS562 from FIG. 50; that is, the VH from the BTLA Fab is added N-terminally to the Fab Chain of XENCS562 and the VL from the BTLA Fab is added N-terminally to the Light Chain of XENCS562.

Anti-BTLA sequences suitable for use as ABDs include SEQ ID NOs: 20885-21503 and SEQ ID NOs: 36707-36738 (s will be understood from those in the art, these sequence identifiers come in “pairs” for the variable heavy and light chains, as will be apparent from the sequence identifiers); anti-BTLA ABD selected from the pairs of SEQ ID NOs:36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and 36735; with the Fab anti-BTLA ABD of XENP20269 (VH SEQ ID NO:20936 and VL SEQ ID NO:20941) finding particular use. In these embodiments, the remainder of the heterodimeric antibody is XENCS563 from FIG. 50; that is, the VH from the BTLA Fab is added N-terminally to the Fab Chain of XENCS563 and the VL from the BTLA Fab is added N-terminally to the Light Chain of XENCS563.

XII. NUCLEIC ACIDS OF THE INVENTION

The invention further provides nucleic acid compositions encoding the heterodimeric bispecific antibodies of the invention as well as the monospecific antibodies outlined herein.

As will be appreciated by those in the art, the nucleic acid compositions will depend on the format and scaffold of the heterodimeric protein. Thus, for example, when the format requires three amino acid sequences, such as for the triple F format (e.g. a first amino acid monomer comprising an Fc domain and a scFv, a second amino acid monomer comprising a heavy chain and a light chain), three nucleic acid sequences can be incorporated into one or more expression vectors for expression. Similarly, some formats (e.g. dual scFv formats such as disclosed in FIG. 1) only two nucleic acids are needed; again, they can be put into one or two expression vectors.

As is known in the art, the nucleic acids encoding the components of the invention can be incorporated into expression vectors as is known in the art, and depending on the host cells used to produce the heterodimeric antibodies of the invention. Generally the nucleic acids are operably linked to any number of regulatory elements (promoters, origin of replication, selectable markers, ribosomal binding sites, inducers, etc.). The expression vectors can be extra-chromosomal or integrating vectors.

The nucleic acids and/or expression vectors of the invention are then transformed into any number of different types of host cells as is well known in the art, including mammalian, bacterial, yeast, insect and/or fungal cells, with mammalian cells (e.g. CHO cells), finding use in many embodiments.

In some embodiments, nucleic acids encoding each monomer and the optional nucleic acid encoding a light chain, as applicable depending on the format, are each contained within a single expression vector, generally under different or the same promoter controls. In embodiments of particular use in the present invention, each of these two or three nucleic acids are contained on a different expression vector. As shown herein and in 62/025,931, hereby incorporated by reference, different vector ratios can be used to drive heterodimer formation. That is, surprisingly, while the proteins comprise first monomer:second monomer:light chains (in the case of many of the embodiments herein that have three polypeptides comprising the heterodimeric antibody) in a 1:1:2 ratio, these are not the ratios that give the best results.

The heterodimeric antibodies of the invention are made by culturing host cells comprising the expression vector(s) as is well known in the art. Once produced, traditional antibody purification steps are done, including an ion exchange chromotography step. As discussed herein, having the pIs of the two monomers differ by at least 0.5 can allow separation by ion exchange chromatography or isoelectric focusing, or other methods sensitive to isoelectric point. That is, the inclusion of pI substitutions that alter the isoelectric point (pI) of each monomer so that such that each monomer has a different pI and the heterodimer also has a distinct pI, thus facilitating isoelectric purification of the “triple F” heterodimer (e.g., anionic exchange columns, cationic exchange columns). These substitutions also aid in the determination and monitoring of any contaminating dual scFv-Fc and mAb homodimers post-purification (e.g., IEF gels, cIEF, and analytical IEX columns).

XIII BIOLOGICAL AND BIOCHEMICAL FUNCTIONALITY OF THE HETERODIMERIC CHECKPOINT ANTIBODIES

Generally the bispecific antibodies of the invention are administered to patients with cancer, and efficacy is assessed, in a number of ways as described herein. Thus, while standard assays of efficacy can be run, such as cancer load, size of tumor, evaluation of presence or extent of metastasis, etc., immuno-oncology treatments can be assessed on the basis of immune status evaluations as well. This can be done in a number of ways, including both in vitro and in vivo assays. For example, evaluation of changes in immune status (e.g. presence of ICOS+ CD4+ T cells following ipi treatment) along with “old fashioned” measurements such as tumor burden, size, invasiveness, LN involvement, metastasis, etc. can be done. Thus, any or all of the following can be evaluated: the inhibitory effects of the checkpoints on CD4+ T cell activation or proliferation, CD8+ T (CTL) cell activation or proliferation, CD8+ T cell-mediated cytotoxic activity and/or CTL mediated cell depletion, NK cell activity and NK mediated cell depletion.

In some embodiments, assessment of treatment is done by evaluating immune cell proliferation, using for example, CFSE dilution method, Ki67 intracellular staining of immune effector cells, and 3H-Thymidine incorporation method,

In some embodiments, assessment of treatment is done by evaluating the increase in gene expression or increased protein levels of activation-associated markers, including one or more of: CD25, CD69, CD137, ICOS, PD1, GITR, OX40, and cell degranulation measured by surface expression of CD107A.

In general, gene expression assays are done as is known in the art.

In general, protein expression measurements are also similarly done as is known in the art.

In some embodiments, assessment of treatment is done by assessing cytotoxic activity measured by target cell viability detection via estimating numerous cell parameters such as enzyme activity (including protease activity), cell membrane permeability, cell adherence, ATP production, co-enzyme production, and nucleotide uptake activity. Specific examples of these assays include, but are not limited to, Trypan Blue or PI staining, 51Cr or 35S release method, LDH activity, MTT and/or WST assays, Calcein-AM assay, Luminescent based assay, and others.

In some embodiments, assessment of treatment is done by assessing T cell activity measured by cytokine production, measure either intracellularly in culture supernatant using cytokines including, but not limited to, IFNγ, TNFα, GM-CSF, IL2, IL6, IL4, IL5, IL10, IL13 using well known techniques.

XIV. EXAMPLES A. Example 1 Investigating In Vitro Binding of XmAb22841

1. 1A: XmAb20717 Simultaneously Occupies PD-1 and CTLA-4 Expressed on the Surface of Cells

HEK293T cells stably expressing CTLA-4 (Crown Bioscience, Santa Clara, Calif.) were transfected with a pCMV6-AC-GFP vector encoding PD-1 (OriGene, Rockville, Md.). 3 days after transfection, cells were treated with indicated test articles for 30 minutes at 4° C. Following incubation, cells were washed two times and stained with Pacific Blue-conjugated XENP20111 (a one-armed scFv-Fc based on the anti-PD-1 arm from XmAb20717) and APC-conjugated XENP20059 (a one-armed Fab-Fc based on the anti-CTLA-4 arm from XmAb20717) for 30 minutes at 4° C. and assayed by flow cytometry. FIGS. 57A-57B and FIG. 58 show receptor occupancy following treatment with the various test articles as depicted by percentage of various populations of GFP+ (CTLA-4+PD−1+) HEK293T cells with unoccupied CTLA-4 and/or PD-1 receptors as indicated by staining. For example, occupancy of CTLA-4 receptors decreases the percentage of PD-1⁺CTLA-4⁺ and PD-1⁻CTLA-4⁺ populations and increases the percentage of PD-1⁺CTLA-4⁺ and PD-1⁻ CTLA-4⁻ populations. FIGS. 57A-57B shows the prevalence of PD-1⁺CTLA-4⁺ and PD-1⁻ CTLA-4⁻. FIG. 58 shows scatter plots depicting the prevalence of various populations following treatment with 12.5 μg/mL of indicated test articles. The data show that XmAb20717 selectively targets cells simultaneously expressing PD-1 and CTLA-4.

B. Example 2: XmAb20717 Enhances Allogeneic Anti-Tumor Responses in Mice

NOD SCID gamma (NSG) mice were engrafted with KG1A-luc cancer cells on Day 0. On Day 21, human PBMCs were engrafted into the intraperitoneally into the mice. After PBMC engraftment, indicated test articles were dosed weekly by intraperitoneal injection (control mice were dosed with PBS) for 4 weeks (or 4 total doses). Tumor growth was monitored by measuring total flux per mouse using an in vivo imaging system (IVIS® Lumina III) and data are shown (days post Pt dose) in FIGS. 59A-59B.

C. Example 3: Investigating In Vitro Binding of XmAb22841

1. XmAb22841 Binding to HEK293T Expressing CTLA-4 and LAG-3

HEK293T cells stably expressing CTLA-4 (Crown Bioscience, Santa Clara, Calif.) were transfected with a pCMV6-AC-GFP vector encoding LAG-3 (OriGene, Rockville, Md.). 3 days after transfection, cells were incubated with of the following test articles at the indicated concentrations for 30 minutes at 4° C.: XmAb22841; XENP16433, a bivalent mAb based on the parental clone from which the anti-CTLA-4 arm of XmAb22841 was derived; XENP16436, a bivalent mAb based on the parental clone from which the anti-LAG-3 arm of XmAb22841 was derived; XENP24893, a one-armed scFv-Fc based on the anti-CTLA-4 arm from XmAb22841; XENP24895, a one-armed Fab-Fc based on the anti-LAG-3 arm from XmAb22841; and XENP15074, a bivalent anti-RSV mAb as a control. Following incubation, cells were washed two times and binding was detected with an anti-human-Fc-A647 conjugated secondary antibody (Jackson Immunoresearch, West Grove, Pa.). MFI indicating binding of test articles to GFP+ cells (i.e. CTLA-4+LAG-3+) are depicted in FIG. 60.

2. Occupancy of CTLA-4 and LAG-3 on HEK293T Expressing CTLA-4 and LAG-3 by XmAb22841

HEK293T cells stably expressing CTLA-4 (Crown Bioscience, Santa Clara, Calif.) were transfected with a pCMV6-AC-GFP vector encoding LAG-3 (OriGene, Rockville, Md.). 3 days after transfection, cells were treated with the following test articles for 30 minutes at 4° C.: XmAb22841, XENP16433, XENP16436, XENP24893, XENP24895, and XENP15074. Following incubation, cells were washed two times and stained with Pacific Blue-conjugated XENP24895 and A647-conjugated XENP23552. FIGS. 61A-61D show receptor occupancy following treatment with the various test articles as depicted by percentage of various populations of GFP+ (CTLA-4+LAG-3+) HEK293T cells with unoccupied CTLA-4 and/or LAG-3 receptors as indicated by staining. For example, occupancy of CTLA-4 receptors decreases the percentage of LAG-3+CTLA-4+ and LAG-3-CTLA-4+ populations and increases the percentage of LAG-3+CTLA-4− and LAG-3-CTLA-4− populations. FIGS. 62A-62B respectively show the amount of unoccupied LAG-3 and CTLA-4 receptors on GFP+ cells following treatment with test articles as indicated by XENP24895 and XENP23552 binding.

3. XmAb22841 Binding to SEB-Stimulated T Cells

Binding of XmAb22841 to T cells was measured in an SEB-stimulated PBMC assay. Staphylococcal Enterotoxin B (SEB) is a superantigen that causes T cell activation and proliferation in a manner similar to that achieved by activation via the T cell receptor (TCR), including expression of checkpoint receptors such as LAG-3 and CTLA-4. Accordingly, human PBMCs from 6 donors were stimulated with 500 ng/mL SEB for 3 days. Cells were then treated with indicated concentrations of the indicated test articles for 30 minutes. Following incubation, cells were washed and stained with an anti-human-Fc-A647 antibody (Jackson Immunoresearch). MFI indicating binding of test articles to CD3+ T cells are depicted in FIGS. 63A-63F respectively for each donor.

The data show that, in PBMCs from each of the donors, XmAb22841 binds more avidly to CD3+ T cells compared to monospecific controls, demonstrating that binding to human T cells is significantly better by bispecific antibody XmAb22841, where each arm monovalently binds a different antigen, than by monospecific antibodies.

D. Example 4: Investigating Cytokine Release and Immune-Related Gene Expression Profiles Following Treatment with Bispecific Checkpoint Antibodies

Human PBMCs were stimulated with 100 ng/mL SEB for 2 days. Following stimulation, cells were washed twice then restimulated with 100 ng/mL SEB and 20 μg/mL indicated test articles. Cell supernatant was collected 24 hours post treatment and assayed for IL-2 and IFNγ by a multiplexed assay on MULTI-SPOT 384-Well Spot plates (Meso Scale Discovery, Rockville, Md.). RNA was extracted from cells and assayed by nCounter® PanCancer Immune Profiling Panel (NanoString Technologies, Seattle, Wash.) which assays 770 target genes covering immune response.

FIG. 64 and FIG. 65 respectively depicts the fold increase in IL-2 and IFNγ following treatment by anti-PD-1 mAb (XENP16432), XmAb20717, and XmAb22841 as well as XmAb22841 in combination with anti-PD-1 mAb, in comparison to anti-RSV mAb (XENP15074). Notably, combination of XmAb22841 with anti-PD-1 mAb resulted in significantly more cytokine release than by either alone, demonstrating the advantage of a triple immune checkpoint blockade. FIG. 66 to FIG. 72 show the fold change in expression of various genes (as determined by Nanostring nCounter®) between the bispecific checkpoint antibodies, anti-PD-1 mAb, and anti-RSV mAb.

E. Example 5: Generation of Anti-PD-1 Clone 1C11

1. Generation and Screening of Anti-PD-1 Hybridoma

To develop additional PD-1 targeting arms, monoclonal antibodies were first generated by hybridoma technology through ImmunoPrecise, through their Standard Method and Rapid Prime Method. For the Standard Method, antigen(s) was injected into 3 BALB/c mice. 7-10 days before being sacrificed for hybridoma generation, the immunized mice received an antigen boost. Antibody titre is evaluated by ELISA on the antigen and the best responding mice are chosen for fusion. A final antigen boost is given 4 days prior to fusion. Lymphocytes from the mice are pooled, purified then fused with SP2/0 myeloma cells. Fused cells are grown on HAT selective Single-Step cloning media for 10-12 days at which point the hybridomas were ready for screening. For the Rapid Prime method, antigen(s) was injected into 3 BALB/c mice. After 19 days, lymphocytes from all the mice are pooled, purified then fused with SP2/0 myeloma cells. Fused cells were grown on HAT selective Single-Step cloning media for 10-12 days at which point the hybridomas were ready for screening. Antigen(s) used were mouse Fc fusion of human PD-1 (huPD-1-mFc), mouse Fc fusion of cyno PD-1 (cynoPD-1-mFc), His-tagged human PD-1 (huPD-1-His), His-tagged cyno PD-1 (cynoPD-1-His) or mixtures thereof.

Anti-PD-1 hybridoma clones generated as described above were subject to two rounds of screening using Octet, a BioLayer Interferometry (BLI)-based method. Experimental steps for Octet generally included the following: Immobilization (capture of ligand or test article onto a biosensor); Association (dipping of ligand- or test article-coated biosensors into wells containing serial dilutions of the corresponding test article or ligand); and Dissociation (returning of biosensors to well containing buffer) in order to determine the affinity of the test articles. A reference well containing buffer alone was also included in the method for background correction during data processing.

For the first round, anti-mouse Fc (AMC) biosensors were used to capture the clones with dips into 500 nM of bivalent human and cyno PD-1-Fc-His. For the second round, clones identified in the first round that were positive for both human and cyno PD-1 were captured onto AMC biosensors and dipped into 500 nM monovalent human and cyno PD-1-His.

2. Characterization of Clone 1C11

One hybridoma clone identified in Example 1 was clone 1C11. DNA encoding the VH and VL of hybridoma clone 1C11 were generated by gene synthesis and subcloned using standard molecular biology techniques into expression vector pTT5 containing human IgG1 constant region with E233P/L234V/L235A/G236del/S267K substitutions to generate XENP21575, sequences for which are depicted in FIG. 9.

3. PD-L1 Blocking with Clone 1C11

Blocking of checkpoint receptor/ligand interaction is necessary for T cell activation. The blocking ability of XENP21575 was investigated in a cell binding assay, with XENP16432 (anti-PD-1 mAb with variable regions of nivolumab), XENP21461 (anti-PD-1 mAb with variable regions of pembrolizumab), and XENP15074 (anti-RSV Mab with variable regions of motavizumab) as controls. HEK293T cells transfected to express PD-1 were incubated with XENP21575, as well as control antibodies. Following incubation, a murine Fc fusion of PD-L1 was added and allowed to incubate. Binding of PD-L1-mFc to HEK293T cells was detected with an anti-murine IgG secondary antibody, data for which are depicted in FIG. 10. The data shows that PD-L1 blocking by XENP21575 was similar to blocking by XENP16432 and XENP21461.

4. T Cell Surface Binding of Clone 1C11

Binding of anti-PD-1 clone 1C11 to T cells was measured in an SEB-stimulated PBMC assay. Staphylococcal Enterotoxin B (SEB) is a superantigen that causes T cell activation and proliferation in a manner similar to that achieved by activation via the T cell receptor (TCR), including expression of checkpoint receptors such as PD-1. Human PBMCs were stimulated with 100 ng/mL for 3 days. Following stimulation, PBMCs were incubated with the indicated test articles at indicated concentrations at 4° C. for 30 min. PBMCs were stained with anti-CD3-FITC (UCHT1) and APC labeled antibody for human immunoglobulin κ light chain. The binding of the test articles to T cells as indicated by APC MFI on FITC+ cells is depicted in FIG. 11.

5. T Cell Activation by Clone 1C11

T cell activation by clone 1C11, as indicated by cytokine secretion, was investigated in an SEB-stimulated PBMC assay. Human PBMCs were stimulated with 500 ng/mL SEB for 2 days. Cells were then washed twice in culture medium and stimulated with 500 ng/mL SEB in combination with indicated amounts of indicated test articles for 24 hours. Supernatants were then assayed for IL-2 and IFNγ by cells, data for which are depicted in FIG. 12A-12B.

6. Humanization of Clone 1C11

Clone 1C11 humanized using string content optimization (see, e.g., U.S. Pat. No. 7,657,380, issued Feb. 2, 2010). DNA encoding the heavy and light chains were generated by gene synthesis and subcloned using standard molecular biology techniques into the expression vector pTT5. Sequences for illustrative humanized variants of clone 1C11 in bivalent antibody format are depicted in FIGS. 13A-13C.

The affinity of XENP22553 was determined using Octet as generally described in Examples. In particular, anti-human Fc (AHC) biosensors were used to capture the test article with dips into multiple concentrations of histidine-tagged PD-1. The affinity result and corresponding sensorgram are depicted in FIG. 14.

7. Stability Optimization of a Humanized Variant of Clone 1C11 in the scFv Format

The variable regions of anti-PD-1 clone 1C11 humanized variant H3L3 (as in XENP22553) were engineered for improved stability (while maintaining affinity) in the context of an scFv, for example, for use in a bispecific antibody. DNA encoding an scFv with the variable heavy and variable light regions of XENP22553 were generated by gene synthesis and subcloned using standard molecular biology techniques into the expression vector pTT5. The C-terminus of the scFv included a polyhistidine tag for purification. A library of scFv variants was then constructed by standard mutagenesis, illustrative sequences for which are depicted in FIG. 15A-15T (although polyhistidine tags have been removed).

Stability of scFv-His was evaluated using Differential Scanning Fluorimetry (DSF). DSF experiments were performed using a Bio-Rad CFX Connect Real-Time PCR Detection System. Proteins were mixed with SYPRO Orange fluorescent dye and diluted to 0.2 mg/mL in PBS. The final concentration of SYPRO Orange was 10×. After an initial 10 minute incubation period of 25° C., proteins were heated from 25 to 95° C. using a heating rate of 1° C./min. A fluorescence measurement was taken every 30 sec. Melting temperatures (Tm) were calculated using the instrument software. Stability results are depicted in FIG. 17A-17Q. The data show that melting temperature (Tm) increased by up to 19° C.

To determine the affinity of the variants, the variable regions from the scFvs were formatted as Fabs in a bivalent IgG1 with E233P/L234V/L235A/G236del/S267K substitutions. Illustrative sequences are depicted in FIGS. 16A-16H. DNA encoding the heavy and light chains were generated by gene synthesis and subcloned using standard molecular biology techniques into pTT5 expression vector containing IgG1 constant regions, and transiently transfected into HEK293E cells. Affinity screens of supernatant were performed using Octet. Anti-human Fc (AHC) biosensors were used to capture 1:2 dilutions of each supernatant to a density of 2.0 nm, and dipped into PD-1-His for KD determination. Affinity results are depicted in FIG. 17A-17Q.

8. Affinity Optimization of a Humanized Variant of Clone 1C11 in the Fab Format

The variable regions of anti-PD-1 clone 1C11 humanized variant H3L3 (as in XENP22553) was generated in the Fab format and engineered for optimized affinity, for example, for use as a bivalent, monospecific antibody or for use in a bispecific antibody.

In a first library, variable heavy and light regions from scFvs generated in Example 4D found to have increased affinity were combined to generate bivalent IgG1 format with E233P/L234V/L235A/G236del/S267K substitutions, illustrative sequences for which are depicted in FIGS. 20A-20L. DNA encoding the heavy and light chains were generated by gene synthesis and subcloned using standard molecular biology techniques into pTT5 expression vector containing IgG1 constant regions, and transiently transfected into HEK293E cells. Antibodies were purified by Protein A chromatography, and affinity screens were performed using Octet. AHC biosensors were used to capture antibodies, and dipped into multiple concentrations of PD-1-His for KD determination. Affinity results are depicted in FIG. 19.

In a second library, additional variants were constructed by standard mutagenesis on the expression vectors encoding either the heavy or light chains of XENP22553. Illustrative sequences for the additional heavy chain and light chain variants are depicted in FIGS. 20A-20L and FIGS. 21A-21G. Expression vectors containing DNA encoding the additional heavy chain variants and DNA encoding the light chain of XENP22553, or DNA encoding the heavy chain of XENP22553 and DNA encoding the additional light chain variants were transiently transfected into HEK293E cells. Affinity screens of supernatant were performed using Octet. Anti-human Fc (AHC) biosensors were used to capture 1:2 dilutions of each supernatant to a density of 2.0 nm, and dipped into PD-1-His for KD determination. Affinity results are depicted in FIGS. 22A-22E. In a follow-up screen, DNA encoding selected antibodies were transfected into HEK293E cells, and antibodies were purified by Protein A chromatography and screened for affinity using Octet. Anti-human Fc (AHC) biosensors were used to capture antibodies, and dipped into multiple concentrations of PD-1-His for KD determination, results for which are depicted in FIG. 23.

Another library was generated as generally described above. Illustrative sequences for resulting antibodies are depicted in FIGS. 24A-24J. DNA encoding selected antibodies were transfected into HEK293E cells, and antibodies were purified by Protein A chromatography and screened for affinity using Octet. Anti-human Fc (AHC) biosensors were used to capture antibodies, and dipped into multiple concentrations of PD-1-His for KD determination, results for which are depicted in FIG. 25.

9. Affinity Screen of Affinity Optimized 1C11 Variants as Determined by Biacore

Affinity of 1C11 variants generated as described above and control mAbs based on nivolumab (XENP16432) and pembrolizumab (XENP21461) were determined using Biacore, a surface plasmon resonance (SPR)-based technology. Experimental steps for Biacore generally included the following: Immobilization (capture of ligand onto a sensor chip); Association (flowing of various concentrations of analyte over sensor chip); and Dissociation (flowing buffer over the sensor chips) in order to determine the affinity of the test articles. A reference flow with buffer alone was also included in the method for background correction during data processing. Binding affinities and kinetic rate constants were obtained by analyzing the processed data using a 1:1 binding model. In particular, anti-PD-1 mAbs were captured onto Protein A sensor chips, and then multiple concentrations of histidine-tagged human PD-1 or histidine tagged cyno PD-1 were flowed over the sensor chips. The resulting dissociation constants (KD) are depicted in FIG. 26.

10. T Cell Surface Binding of Affinity Optimized 1C11 Variants

Binding of affinity optimized 1C11 variants to T cells was measured in an SEB-stimulated PBMC assay. Human PBMCs were stimulated with 500 ng/mL SEB for 3 days. Following stimulation, PBMCs were incubated with the indicated test articles at indicated concentrations 30 min. PBMCs were stained with anti-CD3-FITC (UCHT1) and A647 labeled antibody for human Fc. The binding of the test articles to T cells as indicated by A647 MFI on FITC+ cells is depicted in FIG. 27.

11. Blocking of PD-L1 and PD-L2 Binding to PD-1 by Affinity Optimized 1C11 Variants

The ability of affinity optimized 1C11 variants to block PD-L1 and PD-L2 binding to PD-1 was investigated in a tandem epitope binning assay using the Octet HTX instrument. Experimental steps for Octet were as generally described in Examples. In particular, murine Fc fusion of human PD-1 was loaded onto AMC (anti-mouse Fc capture) biosensors prior to dipping into 100 nM of a first test article (as indicated on the left side of the table depicted in FIG. 28) and then into 100 nM of a second test article (as indicated on the top of the table depicted in FIG. 28). Test articles included affinity optimized variants of humanized clone 1C11 and Fc fusions of PD-L1 and PD-L2 (RnD Systems, Minneapolis, Minn.). The BLI-response of each test article pair was normalized against the response from dipping the biosensor into HBS-EP buffer and then dipping into the test article. The normalized BLI-responses of each pair of test articles are depicted in. If the second test article provided a normalized BLI-response less than 0.4, the binding of the second test article to PD-1 was considered to be blocked by the first test article. If the second test article provided a normalized BLI-response between 0.4 and 0.6, the blocking is considered borderline. If the second test article provided a normalized BLI-response greater than 0.6, the binding of the second test article to PD-1 was considered to not be blocked by the first test article. The data show that each of the anti-PD-1 1C11 variants blocked PD-L1 and PD-L2 binding to PD-1.

F. Example 6: Further Engineering Affinity Optimized 1C11 Variants

We engineered further 1C11 variants to modulate PD-1 affinity using the aforementioned approaches as well as by mixing and matching substitutions that appeared to best modulate affinity. In addition, we combined variant 1C11 variable heavy chains with variant 1C11 variable light chains demonstrating favorable affinity modulation. Illustrative sequences for resulting antibodies are depicted in FIGS. 40A-40BB.

1. Affinity Screen of Additional Affinity-Engineered 1C11 Variants

Affinity of the additional affinity-engineered 1C11 variants were determined using Octet, as generally described above. In particular, AHC biosensor was used to capture the 1C11 variants and dipped into multiple concentrations of His-tagged human PD-1 (as well as His-tagged cynomolgus PD-1 for the data depicted in FIG. 41). The resulting dissociation constants (KD), association rates (ka), and dissociation rates (kd) are depicted in FIG. 41 to FIG. 45, where each Figure depicts separate experimental sets.

2. Induction of Cytokine Secretion by 1C11 Variants in an SEB-Stimulated PBMC Assay

While there was technical variability between experiments as well as between data obtained from Octet or Biacore, the affinity of 1C11_H3L3 (as determined by Octet) was generally in the range of 15-19 nM (from 4/6 experiments). From the various rounds of engineering, we obtained 1C11 variants having much tighter affinities (e.g. XENP26940 having affinity ranging from 0.51-0.74 nM; and XENP28652 having an affinity of 0.77 nM as determined by Octet) as well as variants having much weaker affinities (e.g. XENP26928 having an affinity of 333 nM as determined by Octet) for human PD-1. Accordingly, we investigated T cell activation by the variants with differing affinities, as indicated by cytokine secretion, in an SEB-stimulated PBMC assay. PBMC from 18 unique donors were stimulated with 100 ng/mL SEB for 2 days. Cells were then washed and restimulated with SEB and 20 μg/mL of the test articles. Data depicting IFNγ and IL-2 secretion are depicted respectively in FIG. 46 and FIG. 47. The data suggest a correlation between activity of the 1C11 variants and their affinity as indicated by the weaker binding affinity of XENP26928 and a corresponding weaker induction of cytokine secretion.

In summary, we identified novel anti-PD-1 mAb 1C11, which when humanized as 1C11_H3L3 (XENP22533) has a similar affinity compared to an anti-PD-1 mAb XENP16432 based on nivolumab (respectively 8.6 nM and 4.5 nM as determined by Biacore; respectively ˜18 nM and 10 nM as determined by Octet). Despite the similar affinity, XENP22533 binds T cells more tightly than XENP16432 as depicted in FIG. 11. We engineered XENP22533 to produce variants with modulated affinities over two orders of magnitude toward PD-1 as measured by Octet. This “affinity ladder” should prove useful in identifying the optimal affinity toward PD-1 that can best navigate the complex physiological behaviors of PD-1 receptor recycling, antibody:antigen complex lifetime, and antibody serum half-life. These factors will be explored in future in vivo mouse tumor models.

G. Example 7: Triple Checkpoint Blockade with XmAb22841 and αPD-1 Enhances Cytokine Secretion from SEB-Stimulated Cells

Human PBMCs were stimulated with 100 ng/mL SEB for 2 days. Cells were washed two times and restimulated with 100 ng/mL SEB and 20 μg/mL indicated test articles for 24 hours. Cell supernatants were collected and assayed for IFNγ and IL-2 secretion as depicted in FIG. 29 and FIG. 30. The data show that triple checkpoint blockade enabled by a combination of XmAb22841 and XENP16432 (a bivalent αPD-1 mAb with ablated effector function based on nivolumab) enhance cytokine secretion beyond either XENP16432 or XmAb22841 alone. Notably, the combination of XmAb22841 and XENP16432 enhances cytokine secretion to a similar level as triple checkpoint blockade by a combination of XENP16432, XENP16433 (a bivalent αCTLA-4 mAb with ablated effector function based on ipilimumab), and XENP16436 (a bivalent αLAG-3 mAb with ablated effector function based on 25F7).

H. Example 8: Avidity of XmAb22841 is Responsible for Cytokine Release from MLR

PBMCs from 2 unique donors were mixed (400,000 cells/donor) and incubated with the 20 μg/mL of the indicated test articles for 5 days. Following incubation, cells were assayed for IFNγ as depicted in FIG. 31. In a similar experiment, mixed PBMCs were incubated with various concentrations of indicated test articles for 5 days, and fold induction of IFNγ over PBS are depicted in FIG. 32. The data show that XmAb22841 enhances IFNγ secretion beyond a combination of XENP24895 (one-arm monovalent mAb based on anti-LAG-3 arm of XmAb22841) and XENP24893 (one-arm monovalent mAb based on anti-CTLA-4 arm of XmAb22841) demonstrating that avidity enabled by bivalent binding is necessary for enhancing cytokine release.

I. Example 9: Triple Checkpoint Blockade with XmAb22841 and αPD-1 Enhance GVHD in NSG Mice

NOD SCID gamma (NSG) mice (10 per group) were engrafted via IV-OSP with 10×106 human PBMCs on Day 0. On Day 1, mice were dosed with XENP26842 (a bivalent αPD-1 mAb based on nivolumab with ablated effector function and M428L/N434S Xtend mutations; sequence depicted in FIG. 33), XmAb22841, a combination of XmAb22841 and XENP16432, or PBS for 4 weeks (4 total doses). Blood was drawn on Day 7, 14, and 21 to count various lymphocyte populations as depicted in FIG. 34 (for Day 14) and serum concentrations of IFNγ as depicted in FIG. 35 (for Day 7).

J. Example 10: Triple Checkpoint Blockade with XmAb22841 and αPD-1 Enhances Anti-Tumor Response in Mice

NOD SCID gamma (NSG) mice (10 per group) were engrafted intradermally with 3×106 pp65-expressing MCF-7 cells in the rear flank on Day −14. On Day 0, mice were engrafted intraperitoneally with 5×106 human PBMCs from an HLA matched CMV+ donor that screened positive for T cell pp65 reactivity (or PBS for control mice). Mice were treated weekly with XENP16432, XmAb22841, a combination of XmAb22841 and XENP16432, or PBS (for control mice) for 4 weeks (4 total doses). Tumor volumes were monitored by caliper measurements, data for which are shown (days post 1st dose) in FIGS. 36A-36B. Blood was drawn on Day 7, 12, 19, and 26 and analyzed by flow cytometry to count various lymphocyte populations as depicted in FIGS. 37A-37D. The data show that lymphocyte counts (in particular CD8+ T cells) were similar with or without the various checkpoint inhibitors. However, treatment with the various test articles resulted in notably decreased tumor volume indicating enhanced anti-tumor response from de-repression of T cell activity by checkpoint blockade. Furthermore, the data show that triple checkpoint blockade enabled by the combination treatment with XmAb22841 (targeting CTLA-4 and LAG-3) and XENP16432 (targeting PD-1) synergistically enhanced anti-tumor response over treatment with either XmAb22841 or XENP16432 alone.

K. Example 11: Anti-PD-1 mAb 1C11 Enhances GVHD in PBMC-Engrafted NSG-Mice

In a GVHD study, we investigated the effect of humanized anti-PD-1 mAb 1C11_H3L3 (XENP22553). NSG mice were engrafted i.v. with 10×106 human PBMCs on Day 0, followed by treatment on Days 1, 8, 15, and 21 with the following test articles: PBS control, XENP16432 (an anti-PD-1 antibody based on nivolumab with E233P/L234V/L235A/G236del/S267K ablation variants), and XENP22553. FIG. 38 depicts the change in body weight of mice (as a percentage of initial body weight) over time, and FIGS. 39A-39C depicts human CD45+ cell, CD4+ T cell, and CD8+ T cell counts in mice blood over time.

L. Example 12: Xtend Fc Domain Extends the Half-Life of Anti-PD-1×Anti-CTLA-4 Bispecific Antibody in hFcRn Transgenic Mice

Tg276 transgenic hFcRn mice (hemizygous for hFcRn; n=5) were treated with 2 mg/kg XmAb20717 or XENP20053 (non-Xtend analog of XmAb20717) on Day 0. Whole blood samples were collected 1 hour post-treatment and on Days 2, 5, 8, 12, 15, 19, 22, 16, 29, 33, and 35. Test article concentration was detected using human PD-1 and human CTLA-4 antigen. PK interpretative analysis was performed using Phoenix WinNonlin software (Version 6.4.0.768) with PK parameters for non-compartmental analysis of free drug serum concentration versus time. Pharmacokinetic profile of XmAb20717 and XENP20053 in are depicted in FIGS. 76A-76B; half-life are depicted in FIG. 77; and Cmax are depicted in FIG. 78. Additional PK parameters are summarized in FIG. 79.

M. Example 13: XmAb20717 does not Induce Cytokine Release in Naive T Cells P

BMCs were thawed overnight and treated with 20 μg/mL of indicated soluble or plate bound test articles for 24 hours. Anti-CD3 antibody was clone OKT3. Cell supernatants were then collected and assayed with V-PLEX Proinflammatory Panel 1 Human Kit (Meso Scale, Rockville, Md.). Each point represents a unique human donor tested in technical singlet. Paired t tests were used to determine statistical significance (n.s. signifies a p-value >0.05). The data depicted in FIGS. 80A-80J show that XmAb20717 does not induce cytokine release (A: IFNγ; B: IL-1β; C: IL-2; D: IL-4; E: IL-8; F: IL-6; G: IL-10; H: IL-12p70; I: IL-13; J: TNFα) in naive T cells.

N. Example 14: Further Characterization of Binding by XmAb20717

1. XmAb20717 Binds Human and Cynomolgus CTLA-4 and PD-1

Binding of XmAb20717 to human and cynomolgus CTLA-4 and PD-1 was characterized using Octet, a BioLayer Interferometry (BLI)-based method. Binding affinities were obtained by analyzing the processed data globally using a 1:1 binding model. Octet sensorgrams are shown in FIGS. 81A-81B and FIGS. 82A-82B. The resulting equilibrium dissociation constants (KD), association rate constants (ka), and dissociation constants (kd) are presented in FIG. 83. Affinities for both human and cynomolgus CTLA-4 were measured at approximately 4.1 and 23 nM respectively. Binding affinities for human and cyno PD-1 were 1.4 and 5.5 nM respectively.

2. XmAb20717 Competes for Binding with Ligands of CTLA-4 and PD-1

Binding of CD80 and CD86 to CTLA-4 with and without XmAb20717 and binding of PD-L1 and PD-L2 to PD-1 with and without XmAb20717 was characterized using Octet, a BioLayer Interferometry (BLI)-based method. Octet sensorgrams are shown in FIG. 84 and FIG. 85. In all cases, 100 nM CTLA-4 and 100 nM PD-1 show a binding signal with their ligands (CD80/CD86 and PDL1/PDL2 respectively). In the presence of excess XmAb20717, pre-incubated with CTLA-4 or PD-1 at room temperature for 1 hour prior to the experiment, there is no binding signal observed to any ligands due to the competition of XmAb20717 with CTLA-4 and PD-1 for their ligands CD80/CD86 and PD-L1/PD-L2, respectively.

3. XmAb20717 does not Bind FcγR

Binding of XmAb20717 to human, cynomolgus, and mouse FcγRs was characterized using Octet, a BioLayer Interferometry (BLI)-based method. A comparator antibody was also tested using similar methods: anti-CD19 antibody with a native IgG1 constant region. Octet sensorgrams are shown in FIG. 86 to FIG. 88. While the expected binding patterns for a native human IgG1 antibody were observed for the comparator antibody, no binding for any of the FcγRs was detected for XmAb20717.

4. XmAb20717 Binds Human, Cynomolgus, and Mouse FcRn at pH 6.0

Binding of XmAb20717 to human, cynomolgus, and mouse FcRn at pH 6.0 was characterized using Octet, a BioLayer Interferometry (BLI)-based method. A comparator antibody was also tested using similar methods: XENP20053, an anti-PD1×anti-CTLA4 bispecific antibody containing the same variable regions and engineered constant regions as XmAb20717 but lacking the amino acid substitutions XmAb20717 contains for enhancing FcRn binding. Binding affinities were obtained by analyzing the processed data globally using a 1:1 Langmuir model. Octet sensorgrams are shown FIG. 90. The resulting equilibrium dissociation constants (KD) are presented FIG. 89. Affinities measured for XmAb20717 are tighter than those measured for the comparator, indicating that the Fc substitutions contained in XmAb20717 improve the affinity for FcRn at pH 6.0, the physiologically relevant pH for endosome trafficking.

5. XmAb20717 Simultaneously Binds PD-1 and CTLA-4

Binding of XmAb20717 to both PD1 and CTLA4 antigens was tested using an in-tandem dip approach using BLI technology on the Octet HTX instrument. First, biosensors were loaded with PD-1, then dipped into either XmAb20717 or buffer as a control, and finally, into CTLA-4. FIG. 91 shows the binding sensorgrams which indicate that XmAb20717 can bind to both antigens simultaneously. The XmAb20717 sensorgram continues to increase in signal during the final CTLA4 antigen dip while the control sensorgram with no XmAb20717 loaded remains flat.

O. Example 15: Further In Vitro Characterization of XmAb20717

1. XmAb20717 Promotes Greater IL-2 Secretion from SEB-Stimulated PBMCs Compared to an Anti-PD-1 Antibody

PBMCs from 22 unique donors were stimulated with 500 ng/mL SEB for 48 h. Cells were then washed two times in culture medium and re-stimulated with 500 ng/mL SEB plus 20 μg/mL, of indicated test articles for 18 h. Culture supernatants were collected and assayed for IL-2 concentration by ELISA, data for which are depicted in FIG. 92.

2. XmAb20717 Suppresses IL-2 Secretion from Unstimulated Human PBMCs Compared to an Anti-PD-1 Antibody

Unstimulated PBMCs from 22 unique donors were treated with 20 μg/mL of indicated test articles for 72 h. Culture supernatants were collected and assayed for IL-2 concentration by ELISA, data for which are depicted in FIG. 93.

3. XmAb20717 Promotes Greater IL-2 Secretion from Human Lymphocytes Compared to a Mixture of Component Arms that Comprises XmAb20717

PBMCs from 22 unique donors were stimulated with 500 ng/mL SEB for 48 hours (data from XENP15074 and XENP20717 replicated from FIG. 92). Cells were then washed two times in culture medium and re-stimulated with 500 ng/mL SEB and 20 μg/mL of indicated test articles for 18 hours. Culture supernatants were collected and assayed for IL-2 abundance by ELISA, data for which are depicted in FIG. 94.

P. Example 16: Further Analysis of In Vivo Studies in Murine Models

We further analyzed data from a GVHD study described in an earlier example. FIG. 95 depicts the mean change in body weight of mice (as a percentage of initial body weight) over time. FIG. 96 depicts the survival of mice over time. FIG. 97 depicts the mean IFNγ level over time in the mice. FIGS. 98A-98C depicts human CD45+ cell, CD4+ T cell, and CD8+ T cell counts in mice blood over time.

Q. Example 17: XmAb20717 Combines with PD-L1 Blockade in a GVHD Model

In another GVHD study, we investigated the combination of XmAb20717 with PD-L1 blockade (anti-PD-L1 mAb). NSG mice were engrafted i.v. with 10×106 human PBMCs on Day 0, followed by treatment on Days 1, 8, 15, and 21 with the following test articles: PBS control, XmAb20717, XENP16434 (an anti-PD-L1 antibody based on atezolizumab with E233P/L234V/L235A/G236del/S267K ablation variants; sequences depicted in FIG. 99), and XmAb20717 in combination with XENP16434. FIG. 100 depicts the change in body weight of mice (as a percentage of initial body weight) over time, FIG. 101 depicts the survival of mice over time, and FIGS. 102A-102C depicts human CD45+ cell, CD4+ T cell, and CD8+ T cell counts in mice blood on Day 14.

R. Example 18: Interaction of XmAb20717 with Comparator Anti-PD-1 Antibodies

To determine if pembrolizumab or nivolumab can interfere with the binding activity of XmAb20717, 293T cells stably expressing PD-1-GFP and CTLA-4 were treated with nivolumab or pembrolizumab (16-point 2-fold serial dilutions beginning at 100 μg/mL) for 30 minutes at 4° C. The cells were washed twice with 200 μL ice-cold FACS buffer (3% FBS in PBS), and stained with XmAb20717 conjugated to Alexa647 (16 point 3-fold serial dilutions beginning at 200 μg/mL) on ice for 30 minutes. Cells were then analyzed by FACS for binding by XmAb20717, data for which are depicted in FIG. 103 and FIG. 104. Data depicted in FIG. 103 indicate that nivolumab does not significantly interfere with binding of XmAb20717 to PD-1+CTLA-4+ cells. Data depicted in FIG. 104 indicate that pembrolizumab does interfere with the binding of XmAb20717 to PD-1+CTLA-4+ cells; however, data depicted in FIG. 105 indicate that interference by pembrolizumab can be overcome with high concentrations of XmAb20717. This suggests that XmAb20717 may be administered in a subject in combination with or subsequent to treatment with nivolumab or pembrolizumab.

S. Example 19: XmAb22841 does not Induce Cytokine Release in Naive T Cells and is not Superagonistic

PBMCs were thawed overnight and treated with 20 μg/mL of indicated soluble or plate bound test articles for 24 hours. Anti-CD3 antibody was clone OKT3. Cell supernatants were then collected and assayed with V-PLEX Proinflammatory Panel 1 Human Kit (Meso Scale, Rockville, Md.). Each point represents a unique human donor tested in technical singlet. Paired t tests were used to determine statistical significance (n.s. signifies a p-value >0.05). The data depicted in FIGS. 106A-106J show that XmAb22841 does not induce cytokine release (A: IFNγ; B: IL-1β; C: IL-2; D: IL-4; E: IL-8; F: IL-6; G: IL-10; H: IL-12p70; I: IL-13; J: TNFα) in naive T cells.

Superagonstic properties of XmAb22841 was also assessed by air-drying per the Stebbings protocol (Stebbings R. et al. 2007). Air-drying of test articles was achieved by drying in a SpeedVac™ for 2 hours at room temperature. Human PBMCs were treated for 24 hours with 10 μg of air-dried XmAb22841, and activity was compared to 10 μg of air-dried XENP15074 (anti-RSV negative isotype control) or the superagonist TGN1412 (XENP29154; sequences for which are depicted in FIG. 107). TGN1412 did not possess any activity when bound to the assay plate using an aqueous adsorption method; however, air-dried TGN1412 promoted IFNγ, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, and TNF cytokine secretion from unstimulated human PBMC. In comparison, the cytokine levels in PBMCs treated with air-dried XmAb22841 remained similar to the negative control of air-dried XENP15074 (data shown in FIGS. 108A-108J).

T. Example 20: Further Characterization of Binding by XmAb22841

1. XmAb22841 Binds Human and Cynomolgus CTLA-4 and LAG-3

Binding of XmAb22841 to human and cynomolgus CTLA-4 and LAG-3 was characterized using Octet, a BioLayer Interferometry (BLI)-based method. Binding affinities were obtained by analyzing the processed data globally using a 1:1 binding model. Octet sensorgrams are shown in FIGS. 109A-109B and FIGS. 110A-11B. The resulting equilibrium dissociation constants (KD), association rate constants (ka), and dissociation constants (kd) are presented in FIG. 111. Affinities for both human and cynomolgus CTLA-4 were measured at approximately 4.6 and 17.6 nM respectively. Binding affinities for human and cyno LAG-3 were 1.4 and 1.3 nM respectively.

2. XmAb22841 Competes for Binding with Ligands of CTLA-4 and LAG-3.

Binding of CD80 and CD86 to CTLA-4 with and without XmAb22841 was characterized using Octet, a BioLayer Interferometry (BLI)-based method. Octet sensorgrams are shown in FIG. 112. In both cases, 100 nM CTLA-4 show a binding signal with their ligands (CD80/CD86). In the presence of excess XmAb22841, pre-incubated with CTLA-4 at room temperature for 1 hour prior to the experiment, there is no binding signal observed to any ligands due to the competition of XmAb22841 with CTLA-4 for its ligands CD80/CD86.

Soluble LAG-3 binds to MHC Class II expressed on the surface of cancer del lines. Therefore, we determined if XmAb22841 can block soluble LAG-3 binding to MHCII+ Ramos cells when complexed to XmAb22841. As depicted in FIG. 113, XmAb22841 dose-dependently blocked binding of soluble LAG-3 antigen to Ramos cells.

3. XmAb22841 does not Bind FcγR

Binding of XmAb22841 to human, cynomolgus, and mouse FcγRs was characterized using Octet, a BioLayer Interferometry (BLI)-based method. A comparator antibody was also tested using similar methods: anti-CD19 antibody with a native IgG1 constant region. Octet sensorgrams are shown in FIG. 114 to FIG. 116. While the expected binding patterns for a native human IgG1 antibody were observed for the comparator antibody, no binding for any of the FcγRs was detected for XmAb22841.

4. XmAb22841 Binds Human, Cynomolgus, and Mouse FcRn at pH 6.0

Binding of XmAb22841 to human, cynomolgus, and mouse FcRn at pH 6.0 was characterized using Octet, a BioLayer Interferometry (BLI)-based method. A comparator antibody was also tested using similar methods: XENP22602, an anti-CTLA-4×anti-LAG-3 bispecific antibody containing the same variable regions and engineered constant regions as XmAb22841 but lacking the amino acid substitutions XmAb22841 contains for enhancing FcRn binding. Binding affinities were obtained by analyzing the processed data globally using a 1:1 Langmuir model. Octet sensorgrams are shown FIG. 118. The resulting equilibrium dissociation constants (KD) are presented FIG. 117. Affinities measured for XmAb22841 are tighter than those measured for the comparator, indicating that the Fc substitutions contained in XmAb22841 improve the affinity for FcRn at pH 6.0, the physiologically relevant pH for endosome trafficking.

5. XmAb22841 Simultaneously Binds CTLA-4 and LAG-3

approach using BLI technology on the Octet HTX instrument. First, biosensors were loaded with LAG3, then dipped into either XmAb22841 or buffer as a control, and finally, into CTLA4. FIG. 119 shows the binding sensorgrams which indicate that XmAb22841 can bind to both antigens simultaneously. The XmAb22841 sensorgram continues to increase in signal during the final CTLA4 antigen dip while the control sensorgram with no XmAb22841 loaded remains flat.

U. Example 21: Further Analysis of GVHD by XmAb22841 and PD-1 Blockade

We further analyzed data from a GVHD study investigating triple-checkpoint blockade by XmAb22841 and PD-1 blockade described in an earlier example. FIG. 120 depicts the mean change in body weight of mice (as a percentage of initial body weight) over time. FIG. 121 depicts the survival of mice over time. FIGS. 122A-122B depicts the IFNγ and IL-10 concentrations on Days 7 and 14. 

What is claimed is:
 1. An anti-PD-1 monoclonal antibody comprising: a) a heavy chain comprising, from N- to C-terminal, VH-CH1-hinge-CH2-CH3; and b) a light chain comprising, from N- to C-terminal, VL-CL; wherein the VHCDR1, VHCDR2, VHCDR3, VLCDR1, VLCDR2 and VLCDR3 are selected from the group consisting of the CDRs from XENP26940 in FIG. 24 and the CDRs from XNE28652 in FIG.
 40. 2. An antibody according to claim 1 wherein said VH and VL is selected from the group consisting of the VH and VL from XENP26940 and the VH and VL from XENP28652.
 3. An antibody according to claim 1 or 2 wherein said hinge-CH2-CH3 is an Fc domain selected from the group consisting of the Fc domain from human IgG1, IgG2, IgG3 and IgG4.
 4. An antibody according to claim 3 wherein said Fc domain is a variant human IgG1 domain.
 5. An antibody according to claim 4 wherein said variant human IgG1 domain comprises the amino acid substitutions 427L/434S.
 6. An antibody according to claim 4 or 5 wherein said variant human IgG1 domain comprises ablation variants selected from those depicted in FIG.
 5. 7. An antibody according to claim 3 wherein Fc domain is a variant human IgG4 domain comprising an S228P amino acid substitution.
 8. An antibody according to claim 1 selected from the group consisting of XNE26940 and XENP28652.
 9. A nucleic acid composition comprising: a) a first nucleic acid encoding said heavy chain of any of claims 1 to 8; and b) a second nucleic acid encoding said light chain of any of claims 1 to
 8. 10. An expression vector composition comprising: a) a first expression vector comprising said first nucleic acid of claim 9; and b) a second expression vector comprising said second nucleic acid of claim
 9. 11. An expression vector comprising said first and second nucleic acids of claim
 9. 12. A host cell comprising the expression vector composition of claim 10 or the expression vector of claim
 11. 13. A method of making an anti-PD-1 antibody comprising culturing the host cell of claim 12 under conditions wherein said antibody is expressed, and recovering said antibody.
 14. A method of treating cancer in a patient in need thereof comprising administering the antibody of any of claims 1 to 8 to said patient.
 15. A heterodimeric bispecific antibody comprising: a) a first monomer comprising: i) a single chain Fv domain (scFv) that binds human PD-1, wherein said scFv domain comprises: 1) a first variable heavy domain (VH1); 2) a scFv linker; and 3) a first variable light domain (VL1); and ii) a first variant Fc domain; b) a second monomer comprising: i) a heavy chain comprising a second variable heavy domain (VH2)-CH1-hinge-CH2-CH3; and c) a light chain comprising a second variable light domain (VL2) and a constant light domain (CL); wherein said first variable heavy domain and said first variable light domain form a first antigen binding domain (ABD1) that has sequences selected from the pairs consisting of 1C11[PD-1]_H3.234_L3.144 from XENP25806 in FIG. 15, 1C11[PD-1]_H3.240_L3.148 from XENP25812 from FIG. 15, 1C11[PD-1]_H3.241_L3.148 from XENP25813 in FIG. 15 and 1C11[PD-1]_H3.241_L3.92 from XENP25819 in FIG. 15, and wherein said second variable heavy domain and said second variable light domain form a second ABD (ABD2) that binds to an antigen selected from human CTLA-4, human LAG-3, human TIM-3, human TIGIT, human BTLA and human ICOS.
 16. The heterodimeric bispecific antibody of claim 15, wherein said first monomer comprises, from N- to C-terminal, VH1-scFv linker-VL1-hinge-variant Fc domain.
 17. The heterodimeric bispecific antibody of claim 16, wherein said first monomer comprises, from N- to C-terminal, VL1-scFv linker-VH1-hinge-variant Fc domain.
 18. The heterodimeric antibody of any of claims 15 to 17 wherein said ABD2 binds to human CTLA-4.
 19. The heterodimeric antibody of any of claims 15 to 17 wherein said ABD2 binds to human LAG-3.
 20. The heterodimeric antibody of any of claims 15 to 17 wherein said ABD2 binds to human TIM-3.
 21. The heterodimeric antibody of any of claims 15 to 17 wherein said ABD2 binds to human TIGIT.
 22. The heterodimeric antibody of any of claims 15 to 17 wherein said ABD2 binds to human ICOS.
 23. The heterodimeric antibody of any of claims 15 to 17 wherein said ABD2 binds to human BTLA.
 24. The heterodimeric antibody of claim 18 wherein said anti-CTLA-4 ABD2 has sequences selected from the pairs of SEQ ID NOs:38134 and 38138, 36739 and 36743, 36747 and 36751, 36755 and 36759, 36763 and 36767, 36771 and 36775, 36779 and 36783, 36787 and 36791, 36795 and 36799, 36803 and 36807, and 36811 and 36815 of the sequence listing.
 25. The heterodimeric antibody of claim 19 wherein said anti-LAG-3 ABD2 has sequences selected from the pairs of SEQ ID NOs:32755 and 32760, 36819 and 36823, 36827 and 36831, 36835 and 36839, 36843 and 36847, 36851 and 36855, 36859 and 36863, 36867 and 36871, 36875 and 36879, 36883 and 36887, 36891 and 36895, 36899 and 36903, 36907 and 36911, 36915 and 36919, 36923 and 36927, 36931 and 36935, 36939 and 36943, 36947 and 36951 and 36955 and
 36959. 26. The heterodimeric antibody of claim 20 wherein said anti-TIM-3 ABD2 has sequences selected from the pairs of SEQ ID NOs:36508 and 36513, 35757 and 37591, 37959 and 37599, 37603 and 37607, 37611 and 37615, 37619 and 37623, 37627 and 37631, 37635 and 37639, 37643 and 37647, 37651 and 37655, 37659 and 37663, 37667 and 37671, 37675 and 37679, 37683 and 37687 and 37691 and
 37695. 27. The heterodimeric antibody of claim 21 wherein said anti-TIGIT ABD2 has sequences selected from the pairs of SEQ ID NOs:37435 and 37439, 37443 and 37447, 37451 and 37455, 37459 and 37463, 37467 and 37471, 37475 and 37479, 37483 and 37487, 37491 and 37495, 37499 and 37503, 37507 and 37511, 37515 and 37519, 37523 and 37527, 37531 and 37535, 37539 and 37543, 37547 and 37551, 37555 and 37559, 37563 and 37567, 37571 and 37575 and 37579 and
 37583. 28. The heterodimeric antibody of claim 22 wherein said anti-ICOS ABD2 has sequences selected from the group consisting of: a) the pairs of SEQ ID NOs:26323 and 26328, 27477 and 27452 and 26353 and 26358 from the sequence listing from US2018/0127501; b) the VH and VL sequences of XENCS500 in FIG. 49; c) the VH and VL sequences of XENCS501 in FIG.
 49. 29. The heterodimeric antibody of claim 23 wherein said anti-BTLA ABD2 has sequences selected from the pairs of SEQ ID NOs:20936 and 20941, 36707 and 36711, 36715 and 36719, 36723 and 36727 and 36761 and
 36735. 30. The heterodimeric antibody according to any of claims 15 to 29 wherein said second variant Fc domain comprises amino acid substitutions N208D/Q295E/N384D/Q418E/N421D, wherein said first and second variant Fc domains each comprise amino acid substitutions E233P/L234V/L235A/G236del/S267K; and wherein said first variant Fc domain comprises amino acid substitutions S364K/E357Q and second variant Fc domain comprises amino acid substitutions L368D/K370S, wherein numbering is according to the EU index as in Kabat.
 31. A nucleic acid composition comprising: a) a first nucleic acid encoding said first monomer of any of claims 15 to 30; b) a second nucleic acid encoding said second monomer of any of claims 15 to 30; and c) a third nucleic acid encoding said light chain of any of claims 15 to
 30. 32. An expression vector composition comprising: a) a first expression vector comprising said first nucleic acid of claim 31; b) a second expression vector comprising said second nucleic acid of claim 31; and c) a third expression vector comprising said third nucleic acid of claim
 31. 33. A host cell comprising the expression vector composition of claim
 32. 34. A method of making a heterodimeric antibody comprising culturing the host cell of claim 33 under conditions wherein said antibody is expressed, and recovering said antibody.
 35. A method of treating cancer in a patient in need thereof comprising administering the antibody of any of claims 15 to 30 to said patient. 